Inflammatory Bowel Diseases (IBD) Cannabis Registry

Healthy Clinical Trial

— IBD  

Official title:

Inflammatory Bowel Diseases (IBD) Cannabis Registry

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05578313
• Other study ID #: TLV_0276-19
• Status: Recruiting
• Start date: July 10, 2019
• Est. completion date: July 10, 2024

Study information

• Verified date: October 2022
• Source: Tel-Aviv Sourasky Medical Center
• Contact: Nitsanm Maharshak, Professor
• Phone: +972527360384
• Email: nitsanm[@]tlvmc.gov.il
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The inflammatory bowel diseases (IBDs), ulcerative colitis (UC) and Crohn's disease (CD), are characterized by lifelong relapsing-remitting gastrointestinal inflammation, with symptoms of abdominal pain, diarrhea, and rectal bleeding during active disease. Medical therapy reduces intestinal inflammation and ameliorates symptoms. Medical cannabis has recently been added to the arsenal of symptom-reducing measures in IBD. Though the efficacy of THC and CBD have been established as the two most dominant ingredients of cannabis, the rest of the plant phytochemicals are unknown, and effects on patients are not yet determined.

Description:

Hypothesis (es) and Aims: Prospectively follow IBD patients receiving medical cannabis as treatment of their disease (group 1) in comparison to the following control groups: 2) Healthy patients who do not use cannabis; 3) IBD patients who experience pain and do not use cannabis; 4) IBD patients who do not experience pain and do not use cannabis; 5) IBD patients previously prescribed cannabis and were identified to have positive effect on their disease • Specific aims: a prospective trial to determine whether cannabis can induce remission in patients with IBD. - To identify treatment regimens associated with treatment success in IBD patients. - To identify treatment regimens associated with treatment side effects in IBD patients. - To analyze the optimal drug level for disease management in various IBD patient types. - Study design: - A prospective cohort study - Setting: prospectively collect clinical, behavioral, dietary and environmental data of IBD patients receiving medical cannabis as treatment of their disease. Data will be collected according to a uniform standardized protocol specifically adapted to the needs of the study. - Study population: Eligible IBD patients treated at the IBD clinic in the Tel Aviv Medical Center participating in the study, which have signed an informed consent form and answered to all the study inclusion criteria. Patients will be informed of the study by their treating physician, recruited and followed throughout the follow-up period by study coordinators. This study will include five patient groups: - Group 1 (study group): IBD patients prescribed cannabis as treatment for their bowel disease. - Group 2 (Control group): One hundred healthy patients who do not use cannabis and are not eligible or not interested to commence this intervention. - Group 3 (control group): Up to 100 IBD patient who experience pain and do not use cannabis - Group 4 (control group): Up to 100 IBD patient who do not experience pain and do not use cannabis - Group 5 (Cannabis responders group): up to 100 IBD patients previously prescribed cannabis and were identified to have positive effect on their disease *Study plan: - Among the study group : At baseline, demographic characteristics, medical history, concomitant medication assessment, disease related therapy and failed therapy will be documented. Study visits: Among the study group: recruitment at time 0, after one month (±14 days) of treatment, at three months (±21 days) and at 6 months (±30 days) of therapy (end of study), will be conducted, in which patients will be asked to fill in questionnaires, give biologic samples, undergo clinical, anthropometric and nutritional evaluation and physician assessment and monitoring of therapy, safety and adverse events. The cannabis producing company, composition, quantity and way of consumption will be documented. •Among control group and Cannabis responders group: Healthy controls will be samples once at baseline. All IBD control groups (groups 3-5) will be followed up similarly as the study group and will undergo all sampling and questionnaires, at times 0, 3, 6 months (excluding the 1 month cannabis dose adjustment meeting). Patients will be asked to inform in case of relapse during the follow up period and provide stool and blood samples before therapy is changed. At relapse time point, disease activity index will be recorded and questionnaires will be completed. *Sample collection: Baseline and follow up study visits will include biologic samples collection (blood, feces) from which blood levels of complete blood count (CBC), Albumin, Liver enzymes (ALT, AST, ALP), lipid panel (Total cholesterol, LDL, HDL, triglycerides), creatinine, fasting glucose, C-reactive protein (CRP), drug levels and antibodies (for patients treated with thiopurines and biologics), and fecal levels of Calprotectin will be measured. White blood cells will be separated and stored for m RNA analysis of cannabinoid metabolism. Only RNA fractions will be extracted and analyzed, no DNA will be assessed and no genetic sequencing will be performed . In addition, 10 ml of blood will be drawn for analysis of Th17 cells. CD4 T cells will be purified from peripheral blood of IBD patients by RosetteSep™ Human CD4+ T Cell Enrichment Cocktail kit. STAT3 and IL-17 levels will be analyzed. The samples analysis will be done at Dedi Meiri's lab at the Technion-IIT. Serum, and fecal samples will be stored at -80◦C for future analysis after being authorized by the IRB and by law including cannabis phytochemical analysis (10ml of each) on WBC and on biopsies when available and for fecal microbiome analysis. In appendix A- a detailed list of all tests in each visit. *Endoscopic evaluation: In patients who will undergo a standard of care endoscopic examination for clinical reasons: these will include mucosal and histologic assessment for disease severity (SES-CD and MAYO score for CD and UC patients respectively, PDAI for Pouchitis patients). Mucosal biopsies will be collected from inflamed and healthy areas, and from standard areas of the GI track (table 1), sent for histology assessment and stored for future analysis after being authorized by the IRB and by law. These samples will be stored in RNA Later snapped frozen and stored at -80◦c until analysis. No more than 10 samples will be collected during endoscopy including samples for clinical assessment. Samples from recto-sigmoid junction (20 cm from anus) will be taken in every colonoscopy, regardless of the status of inflammation. *Biologic sample handling: Samples will be stored at -80◦c while coded with no identifying information; access to samples will be restricted to the study staff only. Samples will be stored up to 10 years from final data collection. In this study, serum and fecal samples analyzed will include those gathered from protocol number 0276-19 and from protocol number 0250-17 in patients using medical cannabis only. In the later group, samples will be used only if the patient had agreed for use of samples in other studies other than 0250-17. To both studies, Professor Nitsan Maharshak is PI. *Questionnaires: Baseline and follow up study visits will include data collection from the following: - Documentation of cannabis therapy: consumption method, quantity, THC/CBD concentration and cannabis strain/ barcode of preparation - Food frequency questionnaire - Food diary from last 3 days - Lifestyle questionnaire - Medical management questionnaire (IBD SES- self efficacy scale questionnaire) - Patient reported outcomes (PROMIS) questionnaires - Medical cannabis treatment evaluation questionnaire and Adverse events - Big Five personality traits Anthropometric and nutritional evaluation: - Patients weight (kg), height (m), waist circumference (cm) will be documented at each study visit, and body mass index (BMI) will be calculated. - Nutritional status will be evaluated by a MUST questionnaire *Study endpoints: the study will follow patients throughout 6 months of treatment and follow disease remission (clinical/biochemical) or exacerbation. - Disease remission: - Reduction in appropriate clinical scores - Decrease in serum CRP or fecal CLP - Endoscopic remission - Disease exacerbation: - Increase in appropriate clinical score - Increase in fecal calprotectin levels (>250mg/gr OR 100 units higher than baseline levels) - Emergency room visit due to disease symptoms, hospitalization, non-elective surgery. - Diagnosis of active disease by endoscopy or imaging - Medical treatment change by treating physician - Statistical analysis: Statistical analyses will be performed using SPSS version 23.0 for Windows. Patients who adhere to the study's protocol (defined as preforming ≥ 80% of exercises) will be included in data analysis. An intention-to-treat analysis will include patients excluded because of non-adherence to the intervention. Descriptive statistics will be used to describe the distribution of variables associated with characteristics of the study sample. Continuous variables will be presented as means± SD and dichotomous/categorical variables as proportions. The normality of the distribution of continuous variables will be tested by the Kolmogorov-Smirnov test. If normality is rejected, non-parametric tests will be used. Univariate analysis: To test the association between continuous variables with normal distribution, the Pearson correlation coefficient will be performed. To test associations between continuous variables which do not distribute normally or for ordinal variable, the spearman correlation coefficient will be used. To test differences in continuous variables between the treatments arms the t-test for independent groups (or Mann-Whitney test for non-normally distributed variables) will be performed. For comparison of dichotomous or categorical variables the Chi-square test will be performed. To compare baseline to end of treatment parameters within arms for continuous variables the t-test for dependent groups will be performed (or Wilcoxson test for non-normally distributed variables), in dichotomous/categorical variables the McNemar Test will be performed. To test differences in continuous variables between the treatment groups in numbers of time points the Mix model for repeated measures will be performed. To test differences in dichotomous/categorical variables between the treatment groups in numbers of time points Generalized estimating equation will be performed.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 1000
• Est. completion date: July 10, 2024
• Est. primary completion date: July 10, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

Patients (male and female, age 18-80 years) diagnosed with Crohn's disease (CD), ulcerative colitis (UC) or pouchitis, and healthy volunteers. All patients will sign an informed consent form. IBD patients who are recruited to group 3 will be included if they report mild-severe abdominal pain in clinical questioning of clinical activity (Harvey-Bradshaw index). Healthy participants recruited to group 2 will be healthy volunteers with no prior/current use of medical cannabis

Exclusion Criteria:

• Inability to sign an informed consent and complete the study protocol
• Unstable or uncontrolled medical disorder, or severe systemic disease (other than IBD)
• Participating in clinical interventional trial unrelated to cannabis derived preparations
• Ileostomy/ colostomy
• Pregnancy or intent to become pregnant in the next 6 month or breast feeding during the study

Related Conditions & MeSH terms

• Crohn Disease
• Healthy
• Inflammatory Bowel Diseases
• Pouchitis
• Ulcerative Colitis

Intervention

Drug:
• Medical Cannabis
Patients will be observed throughout their treatment with medical cannabis, prescribed to them by for clinically treating their disease (treatment is not an intervention of the study).

Locations

Country	Name	City	State
Israel	Dep. of Gastroenterology, Tel Aviv Sourasky Medical Center	Tel Aviv

Sponsors (1)

Lead Sponsor	Collaborator
Eli Sprecher, MD

Country where clinical trial is conducted

Israel, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Assess the effect of cannabis treatment on pain levels using visual analog scale (VAS) in patients with IBD, after 1 month of treatment	Pain levels will be measured using pain visual analog scale (VAS); VAS scale range from 0 to 10, where 0 means no pain and higher score means worse pain	week 4
Other	Assess the effect of cannabis treatment on pain levels using visual analog scale (VAS) in patients with IBD, after 3 month of treatment	Pain levels will be measured using pain visual analog scale (VAS); VAS scale range from 0 to 10, where 0 means no pain and higher score means worse pain	week 12
Other	Assess the effect of cannabis treatment on pain levels using visual analog scale (VAS) in patients with IBD, after 6 month of treatment	Pain levels will be measured using pain visual analog scale (VAS); VAS scale range from 0 to 10, where 0 means no pain and higher score means worse pain	week 24
Other	Assess the effect of cannabis treatment on sleep quality using the Pittsburgh Sleep Quality Index (PSQI) in patients with IBD after 1 month of treatment	Sleep quality will be measured using the PSQI; PSQI has a range of 0-21; higher score indicate worse sleep quality.	week 4
Other	Assess the effect of cannabis treatment on sleep quality using the Pittsburgh Sleep Quality Index (PSQI) in patients with IBD after 3 month of treatment	Sleep quality will be measured using the PSQI; PSQI has a range of 0-21; higher score indicate worse sleep quality.	week 12
Other	Assess the effect of cannabis treatment on sleep quality using the Pittsburgh Sleep Quality Index (PSQI) in patients with IBD after 6 month of treatment	Sleep quality will be measured using the PSQI; PSQI has a range of 0-21; higher score indicate worse sleep quality.	week 24
Other	Assess the safety of cannabis treatment in patients with IBD after 1 month of treatment	The safety of cannabis treatment will be measured using Common Terminology Criteria for Adverse Events (CTCAE)	4 weeks
Other	Assess the safety of cannabis treatment in patients with IBD after 3 month of treatment	The safety of cannabis treatment will be measured using Common Terminology Criteria for Adverse Events (CTCAE)	12 weeks
Other	Assess the safety of cannabis treatment in patients with IBD after 6 month of treatment	The safety of cannabis treatment will be measured using Common Terminology Criteria for Adverse Events (CTCAE)	24 weeks
Other	Assess the effect of cannabis treatment on quality of life using medical management questionnaire (IBD self-efficacy scale) in patients with IBD	Quality of life will be measured using IBD self-efficacy scale questionnaire; The overall score of the IBD-SES ranges from 29 to 290 with a lower score indicating lower SE.	week 24
Other	Assess the effect of cannabis treatment on quality of life Patient Reported Outcomes (PROMIS) questionnaire in patients with IBD	Quality of life will be measured using Patient Reported Outcomes (PROMIS) questionnaire; PROMIS measures use T-scores. A higher PROMIS T-score represents more of the concept being measured (negative or positive)	week 24
Other	Assess personality traits of patients with IBD favoring cannabis treatment using the Big Five personality traits questionnaire	Personality traits will be measured using the Big Five personality traits questionnaire; Each personality type will have a score between 0-40. Higher scores equal stronger personality type.	week 24
Primary	Determine patients clinical response rates using Harvey-Bradshaw Index (HBI) in Crohn's disease patients receiving cannabis at week 4	Disease clinical response will be measured as the change in HBI scores from baseline to week 4.; A clinical response is defined as reduction of at least 3 points in HBI score, ?HBI>3 in patients with baseline HBI>7.; Harvey-Bradshaw Index (HBI) is a tool for assessing the degree of illness (activity) in patient's with Crohn's disease. Higher score means higher disease activity and severity. A drop > 3 is considered a clinical response.	week 4
Primary	Determine the clinical response rates using SCCAI (Simple Clinical Colitis Activity Index) in patients with Ulcerative Colitis receiving cannabis at week 4	Disease clinical response will be measured as the change in SCCAI scores from baseline to week 4.; A clinical response is defined as reduction of at list 30% in SCCAI score, ?SCCAI>30% for Ulcerative Colitis; SCCAI (Simple Clinical Colitis Activity Index) is used to assess the severity of symptoms in people who suffer from ulcerative colitis. Score range from 0 to 19 points 0	week 4
Primary	Determine patients clinical response rates using Harvey-Bradshaw Index (HBI) in Crohn's disease patients receiving cannabis at week 12	Disease clinical response will be measured as the change in HBI scores from baseline to week 12.; A clinical response is defined as reduction of at least 3 points in HBI score, ?HBI>3 in patients with baseline HBI>7.; Harvey-Bradshaw Index (HBI) is a tool for assessing the degree of illness (activity) in patient's with Crohn's disease. Higher score means higher disease activity and severity. A drop > 3 is considered a clinical response.	week 12
Primary	Determine the clinical response rates using SCCAI (Simple Clinical Colitis Activity Index) in patients with Ulcerative Colitis receiving cannabis at week 12	Disease clinical response will be measured as the change in SCCAI scores from baseline to week 12.; A clinical response is defined as reduction of at list 30% in SCCAI score, ?SCCAI>30% for Ulcerative Colitis; SCCAI (Simple Clinical Colitis Activity Index) is used to assess the severity of symptoms in people who suffer from ulcerative colitis. Score range from 0 to 19 points 0	week 12
Primary	Determine patients clinical response rates using Harvey-Bradshaw Index (HBI) in Crohn's disease patients receiving cannabis at week 24	Disease clinical response will be measured as the change in HBI scores from baseline to week 24.; A clinical response is defined as reduction of at least 3 points in HBI score, ?HBI>3 in patients with baseline HBI>7.; Harvey-Bradshaw Index (HBI) is a tool for assessing the degree of illness (activity) in patient's with Crohn's disease. Higher score means higher disease activity and severity. A drop > 3 is considered a clinical response.	Week 24
Primary	Determine the clinical response rates using SCCAI (Simple Clinical Colitis Activity Index) in patients with Ulcerative Colitis receiving cannabis at week 24	Disease clinical response will be measured as the change in SCCAI scores from baseline to week 24.; A clinical response is defined as reduction of at list 30% in SCCAI score, ?SCCAI>30% for Ulcerative Colitis; SCCAI (Simple Clinical Colitis Activity Index) is used to assess the severity of symptoms in people who suffer from ulcerative colitis. Score range from 0 to 19 points 0	Week 24
Secondary	Determine clinical remission rates using Harvey-Bradshaw Index (HBI) in Crohn's disease patients receiving cannabis at weeks 4	Disease remission will be defined by HBI <5; Higher HBI clinical score means higher disease severity: Remission<5 Mild Disease 5-7 Moderate Disease 8-16 Severe Disease >16	week 4
Secondary	Determine clinical remission rates using SCCAI (Simple Clinical Colitis Activity Index) in patients with Ulcerative Colitis receiving cannabis at week 4	Disease remission will be defined by SCCAI <3; SCCAI (Simple Clinical Colitis Activity Index) score range from 0 to 19. Higher score means higher disease severity.	week 4
Secondary	Determine clinical remission rates using Harvey-Bradshaw Index (HBI) in Crohn's disease patients receiving cannabis at weeks 12	Disease remission will be defined by HBI <5; Higher HBI clinical score means higher disease severity: Remission<5 Mild Disease 5-7 Moderate Disease 8-16 Severe Disease >16	week 12
Secondary	Determine clinical remission rates using SCCAI (Simple Clinical Colitis Activity Index) in patients with Ulcerative Colitis receiving cannabis at week 12	Disease remission will be defined by SCCAI <3; SCCAI (Simple Clinical Colitis Activity Index) score range from 0 to 19. Higher score means higher disease severity.	week 12
Secondary	Determine clinical remission rates using Harvey-Bradshaw Index (HBI) in Crohn's disease patients receiving cannabis at weeks 24	Disease remission will be defined by HBI <5; Higher HBI clinical score means higher disease severity: Remission<5 Mild Disease 5-7 Moderate Disease 8-16 Severe Disease >16	week 24
Secondary	Determine clinical remission rates SCCAI (Simple Clinical Colitis Activity Index) in patients with Ulcerative Colitis receiving cannabis at week 24	Disease remission will be defined by SCCAI <3; SCCAI (Simple Clinical Colitis Activity Index) score range from 0 to 19. Higher score means higher disease severity.	week 24
Secondary	Determine endoscopic response rates using Simple Endoscopic Score for Crohn Disease (SES-CD) in patients with Crohn's disease receiving cannabis at weeks 4	Endoscopic response will be defined as decrease of =50% in SES-CD score from baseline to week 4; Higher SES-CD score means higher disease activity and severity. A drop > 50% is considered an endoscopic response	week 4
Secondary	Determine endoscopic response rates using Mayo score in patients with Ulcerative Colitis receiving cannabis at weeks 4	Endoscopic response will be defined as reduction in Endoscopic Mayo score = 1 for Ulcerative Colitis; Endoscopic Mayo score range from 0-3. Higher score means higher disease severity	week 4
Secondary	Determine endoscopic response rates using Simple Endoscopic Score for Crohn Disease (SES-CD) in patients with Crohn's disease receiving cannabis at weeks 12	Endoscopic response will be defined as decrease of =50% in SES-CD score from baseline to week 12; Higher SES-CD score means higher disease activity and severity. A drop > 50% is considered an endoscopic response	week 12
Secondary	Determine endoscopic response rates using Mayo score in patients with Ulcerative Colitis receiving cannabis at weeks 12	Endoscopic response will be defined as reduction in Endoscopic Mayo score = 1 for from baseline to week 12; Endoscopic Mayo score range from 0-3. Higher score means higher disease severity	week 12
Secondary	Determine endoscopic response rates using Simple Endoscopic Score for Crohn's Disease (SES-CD) in patients with Crohn's disease receiving cannabis at weeks 24	Endoscopic response will be defined as decrease of =50% in SES-CD score from baseline to week 24; Higher SES-CD score means higher disease activity and severity. A drop > 50% is considered an endoscopic response	week 24
Secondary	Determine endoscopic response rates using Mayo score in patients with Ulcerative Colitis receiving cannabis at weeks 24	Endoscopic response will be defined as reduction in Endoscopic Mayo score = 1 for from baseline to week 24; Endoscopic Mayo score range from 0-3. Higher score means higher disease severity	week 24
Secondary	Determine endoscopic remission rates using Simple Endoscopic Score for Crohn's Disease (SES-CD) in patients with Crohn's disease receiving cannabis at week 4	Endoscopic remission will be defined as SES-CD<4 for Crohn's disease; SES-CD ranges from a minimum score o and has no high limit. Higher SES-CD score means higher disease severity and activity.	week 4
Secondary	Determine endoscopic remission rates using Mayo score in patients with Ulcerative Colitis receiving cannabis at weeks 4	Endoscopic remission will be defined as Endoscopic Mayo score = 0 for ulcerative colitis; Endoscopic Mayo score range from 0-3. Higher score means higher disease severity	week 4
Secondary	Determine endoscopic remission rates using Simple Endoscopic Score for Crohn's Disease (SES-CD) in patients with Crohn's disease receiving cannabis at week 12	Endoscopic remission will be defined as SES-CD<4 for Crohn's disease; SES-CD ranges from a minimum score o and has no high limit. Higher SES-CD score means higher disease severity and activity.	week 12
Secondary	Determine endoscopic remission rates using Mayo score in patients with Ulcerative Colitis receiving cannabis at weeks 12	Endoscopic remission will be defined as Endoscopic Mayo score = 0 for ulcerative colitis; Endoscopic Mayo score range from 0-3. Higher score means higher disease severity	week 12
Secondary	Determine endoscopic remission rates using Simple Endoscopic Score for Crohn's Disease (SES-CD) in patients with Crohn's disease receiving cannabis at week 24	Endoscopic remission will be defined as SES-CD<4 for Crohn's disease; SES-CD ranges from a minimum score o and has no high limit. Higher SES-CD score means higher disease severity and activity.	week 24
Secondary	Determine endoscopic remission rates using Mayo score in patients with Ulcerative Colitis receiving cannabis at weeks 24	Endoscopic remission will be defined as Endoscopic Mayo score = 0 for Ulcerative Colitis; Endoscopic Mayo score range from 0-3. Higher score means higher disease severity	week 24