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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02940054
Other study ID # 1414
Secondary ID
Status Recruiting
Phase N/A
First received October 17, 2016
Last updated October 21, 2016
Start date February 2015
Est. completion date March 2018

Study information

Verified date October 2016
Source Istituto Clinico Humanitas
Contact Silvio Danese, MD, PhD
Email IBDclinicaltrials@humanitas.it
Is FDA regulated No
Health authority Italy: Ethics Committee
Study type Observational

Clinical Trial Summary

Observational prospective study to validate a new index for early diagnosis of Crohn's disease (CD)


Description:

The study will be conducted in Italian referral centers for Crohn's disease and will involve general practitioners (GPs) for RED-Flags Index validation.

The project is divided into two phases.

1. retrospective phase (4 weeks). All the general practitioners participating to the study will extrapolate from their patient's database, the total number of patients with a Crohn's disease diagnosis performed in the past. The date of diagnosis will be indicated. No other information will be provided. These data will be then analyzed to obtain, for each GP, the total number of CD diagnosed in each semester.

2. retrospective phase (6 months). GPs will administer the RED-Flags questionnaire to all patients that meet inclusion and exclusion criteria, after informed consent signature. All these patients will be then referred to the nearest referral center, to be evaluated by a gastroenterologist specialized in CD, to confirm or exclude a CD.


Recruitment information / eligibility

Status Recruiting
Enrollment 600
Est. completion date March 2018
Est. primary completion date December 2017
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

1. at least one of the following symptoms, for at least 4 weeks (either continuous or intermittent)

1. diarrhea (>3 bowel movements per day)

2. nocturnal diarrhea

3. weight loss (=5% of usual body weight)

4. abdominal pain (chronic or intermittent)

5. perianal lesions or fistulae or perianal abscess (hemorrhoidal diseases excluded)

2. In the opinion of the investigator, the subject is capable of understanding and complying with protocol requirements. The subject signs and dates a written, informed consent form and any required privacy authorization prior to the initiation of any study procedures.

Exclusion Criteria:

1. known diagnosis of Crohn's disease, ulcerative colitis, chronic diverticulosis or any other gastrointestinal disease

2. any clinical condition that, in the opinion of the investigator, can alter stud results

3. inability to understanding and complying with protocol requirements

4. informed consent not signed and dated by the subject

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
Red-flags questionnaire
A questionnaire composed by 8 items will be administered by GPs to those patients and they will be referred to a gastroenterologist with expertise in CD. All those patients will be evaluated, as per usual practice, to confirm or exclude Crohn's disease.

Locations

Country Name City State
Italy Humanitas Gavazzeni Bergamo BG

Sponsors (3)

Lead Sponsor Collaborator
Istituto Clinico Humanitas IG-IBD talian Group for Inflammatory Bowel Diseases, Takeda

Country where clinical trial is conducted

Italy, 

References & Publications (1)

Danese S, Fiorino G, Mary JY, Lakatos PL, D'Haens G, Moja L, D'Hoore A, Panes J, Reinisch W, Sandborn WJ, Travis SP, Vermeire S, Peyrin-Biroulet L, Colombel JF. Development of Red Flags Index for Early Referral of Adults with Symptoms and Signs Suggestive of Crohn's Disease: An IOIBD Initiative. J Crohns Colitis. 2015 Aug;9(8):601-6. doi: 10.1093/ecco-jcc/jjv067. Epub 2015 Apr 23. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Sensibility of the Red Flags Index Sensibility, specificity, accuracy, positive and negative likelihood ratio measurement at enrollment No
Secondary Percentage of early diagnosed Percentage of early diagnosed of Crohn's Disease in the 6 months of prospective use of the tool 6 months of prospective period No
Secondary Cut-off for Crohn's disease diagnosis Identification of the cut-off associated with an early diagnosis of Crohn's disease at enrollment No
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