Effect of Fecal Microbiota Transplantation in Slow Transit Constipation

Slow Transit Constipation Clinical Trial

— FMTSTC  

Official title:

A Study of Efficacy, Safety and Durability of Fecal Microbiota Transplantation in Adult Patients With Slow Transit Constipation

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT02301221
• Other study ID #: RIGS-FMT-STC-2014
• Status: Active, not recruiting
• Phase: Phase 2
• First received: November 11, 2014
• Last updated: November 3, 2016
• Start date: March 2015
• Est. completion date: December 2016

Study information

• Verified date: November 2016
• Source: Jinling Hospital, China
• Contact: n/a
• Is FDA regulated: No
• Health authority: China: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the effect of fecal microbiota transplantation in adults with slow transit constipation.

Description:

Constipation is a chronic disease estimated to affect about 10% - 15% of the worldwide general population. Constipation frequency appears to augment with increasing age, particularly after 65 years old.

Recent evidence in the literature and collected in our laboratory confirm that constipation can be a consequence of intestinal dysbiosis, with an increase of potentially pathogenic microorganisms and a decrease of potentially beneficial microorganisms. These alterations may affect the motility and metabolic environment of colon, especially the production of short chain fatty acids (SCFAs).

A new and under-explored method to manipulate the gastrointestinal microbiota involves fecal microbiota transplantation (FMT). There has been growing interest in the use of fecal microbiota for the treatment of patients with chronic gastrointestinal infections (e.g. CDI) and other extraintestinal conditions (e.g. IBD). Similarly, we suppose that reshaping the gut microbiome with FMT would be effective for patients with slow transit constipation.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 60
• Est. completion date: December 2016
• Est. primary completion date: March 2016
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Chronic constipation according to Rome III criteria, defined as two or fewer spontaneous, complete bowel movements (SCBMs) per week for a minimum of 6 months;

• Age = 18 years;

• BMI: 18.5-25 kg/m2;

• Slow colonic transit confirmed by colonic transit test (colonic transit time (CTT) > 48 hours);

• Normal anorectal manometry with no evidence of dyssynergia and confirmed ability to expel rectal balloon;

• No radiographic evidence of functional (i.e. pelvic floor dyssynergia) or anatomical (i.e. significant rectocele and intussusception) impediment to the expulsion of the radio-opaque contrast;

• Disease duration > 1 year;

• Traditional treatment with dietary modification, laxatives (including osmotic and stimulant laxatives), and biofeedback tried over the past 6 months without success;

Exclusion Criteria:

• Bowel constipation due to innate factor (i.e. megacolon) or secondary interventions (i.e. drugs, endocrine, metabolic, neurologic or psychologic disorders);

• History or evidence of gastrointestinal diseases (i.e. obstruction, cancer, inflammatory bowel diseases) ;

• Previous abdominal surgery, except cholecystectomy, appendicectomy, tubal ligation and cesarean section;

• Previous proctological or perianal surgery;

• A constipation condition meeting the Rome III criteria for IBS or functional abdominal pain syndrome;

• Pregnant or breast-feeding women;

• Infection with enteric pathogen;

• Usage of probiotics, prebiotics and/or synbiotics within the last month;

• Usage of antibiotics and/or PPIs within the last 3 months;

• Smoking or alcohol addiction within the last 3 months;

• Uncontrolled hepatic, renal, cardiovascular, respiratory or psychiatric disease;

• Disease or therapy with drugs (i.e. antidepressants, opioid narcotic analgesics, anticholinergics, calcium antagonists, nitrates, antimuscarinics) that, in the opinion of the investigator, could affect intestinal transit and microbiota.

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Constipation
• Slow Transit Constipation

Intervention

Procedure:
• Fecal microbiota transplantation (FMT)
Standardized Frozen Fecal Microbiota will be infused via nasointestinal tube.

Drug:
• Vancomycin and bowel lavage
An initial vancomycin regimen (500 mg orally two times per day for 3 days), followed by bowel lavage before the infusion of a solution of donor fecal microbiota.

Locations

Country	Name	City	State
China	Department of Generay Surgery, Jinling hosptal, Medical School of Nanjing University	Nanjing	Jiangsu

Sponsors (1)

Lead Sponsor	Collaborator
Jinling Hospital, China

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Proportion of patients having on average three or more SCBMs/week	Proportion of patients having on average three or more spontaneous, complete bowel movements (SCBMs) per week was evaluated at baseline and over the week interval 3-4, 9-12 and 21-24.	24 weeks	No
Secondary	Bowel habit assessments	Patients kept daily diaries about times of bowel movements each day, stool consistency, degree of straining severity during defecation, and degree of sensation of incompleteness of evacuation.	24 weeks	No
Secondary	Constipation-related symptoms assessments	Constipation-related symptoms were evaluated using the validated Patient Assessment of Constipation Symptoms (PAC-SYM) questionnaire at baseline and at week 4, 12, and 24.	24 weeks	No
Secondary	Quality-of-Life assessments	Quality-of-Life was evaluated using the validated Patient Assessment of Constipation Quality of Life (PAC-QOL) self-report questionnaire at baseline and at week 4, 12, and 24.	24 weeks	No
Secondary	Colonic transit time measurements	Colonic transit time (CTT) was measured at baseline and at week 4, 12 and 24 with the Metcalf method.	24 weeks	No
Secondary	Usage of laxatives or enemas as rescue medication	If patients did not have a bowel movement for 3 or more consecutive days, they were permitted to take up to 20 g of Macrogol 4000 powder (Forlax). If ineffective, enema were used. Patients kept daily diaries about the rescue medication when used.	24 weeks	No
Secondary	Adverse events	Adverse events include fever, diarrhea, abdominal pain, increased bloating, borborygmi, flatulence, nausea, vomiting, nasopharyngitis, and any other disorders.	24 weeks	Yes