Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02877654
Other study ID # 2015/174/HP
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 2, 2017
Est. completion date May 20, 2021

Study information

Verified date September 2021
Source University Hospital, Rouen
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Increased intestinal permeability is one of the main pathophysiological mechanisms involved in irritable bowel syndrome. The expression of some intestinal tight junction proteins is decreased mostly in IBS-diarrhoea patients. This decrease is correlated with increased intestinal permeability. Currently, no test used in clinical practice could assess intestinal permeability. We hypothesis plasmatic zonulin could reflect intestinal permeability in IBS patients.


Description:

The goal of our study is to look for a correlation between plasmatic zonulin and increased colonic permeability (assessed by the expression of intestinal tight junction proteins by western blot) in IBS patients and to look for a role of intestinal low-grade inflammation and microbiota. Population : IBS patients with diarrhoea or IBS with constipation or mixed with worsening of symptoms Outcomes measures : Plasmatic zonulin (ELISA kit) Occludin expression in colonic biopsies (western blot)


Recruitment information / eligibility

Status Completed
Enrollment 67
Est. completion date May 20, 2021
Est. primary completion date May 20, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - IBS-Diarrhoea, IBS-constipation or alternating with recent worsening of symptoms, according to Rome III criteria - Effective contraception since 1 month for women in childbearing age Exclusion Criteria: - Patients with organic and/or inflammatory digestive disease - IBS with constipation or alternating without clinical warning sign - Treatment such as anti-inflammatory, probiotic in the last three months - Severe renal failure - Hypersensitivity to Normacol - Patient with blood dyscrasia disorder known or identified, anticoagulant or antiplatelet treatments - Anal pathology (anal fissure, hemorrhoidal thrombosis) - Pregnant or breastfeeding women - Person with administrative or judicial decision or under legal protection measure - Patient participating in another trial in the last two weeks

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
colonoscopy with biopsies in the left colon to assess intestinal permeability
Eleven colonic biopsies are taken in the left colon during colonoscopy. Intestinal permeability is assessed by western blot, qPCR and immunofluorescence for claudin; occludin and ZO-1. One blood sample is taken to assess plasmatic zonulin (ELISA kit).

Locations

Country Name City State
France Rouen University Hospital Rouen

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Rouen

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary occludin level expression in left colonic biopsies occludin expression is measured using western blot (for proteins), q RT-PCT (for RNA) and IF (for localization).
Plasmatic zonulin is measured in plasma using ELISA kit.
day 1
Primary plasmatic zonulin expression Plasmatic zonulin expression is done using ELISA kit day 1
Secondary Claudin and ZO-1 level expression in left colonic biopsies Claudin and ZO-1 expression is measured using western blot (for proteins), q RT-PCT (for RNA) and IF (for localization) day 1
Secondary Faecal calprotectin level Level is assessed on stool sample by ELISA kit in µg/g day 1
Secondary Quality of life (GIQLI) Evaluation of quality of life using the validated score : french version of the Gastrointestinal Quality of Life Index (GIQLI). day 1
Secondary Abdominal symptoms Abdominal symptoms of IBS are assessed with IBS symptom severity scale. day 1
Secondary Anxiety and depression levels Anxiety and depression are assessed with the Hospital anxiety and depression scale. day 1
See also
  Status Clinical Trial Phase
Completed NCT03720314 - Microbiota Profiling in IBS
Recruiting NCT06166563 - Exercise, Irritable Bowel Syndrome and Fibromyalgia N/A
Completed NCT05213910 - Study of a Management Strategy of Functional Bowel Disordes Related to Irritable Bowel Syndrome (IBS) With a Mixture of 8 Microbiotic Strains N/A
Recruiting NCT05985018 - Traditional Dietary Advice Vs. Mediterranean Diet in IBS N/A
Completed NCT04486469 - Efficacy of Physiotherapy Techniques on Irritable Bowel Syndrome (IBS). Pilot Study. N/A
Completed NCT06407609 - Positive Outcomes of the Supplementation With Lecithin-based Delivery Form of Curcuma Longa and of Boswellia Serrata in IBS N/A
Completed NCT04656730 - Effect of STW5 (Iberogast ®) and STW5-II (Iberogast N®) on Transit and Tolerance of Intestinal Gas Phase 4
Completed NCT04145856 - Combination of Alverine-simeticone and i3.1 Probiotic in IBS-D and IBS-M in Mexico Phase 4
Recruiting NCT04138225 - The Ecological Role of Yeasts in the Human Gut
Active, not recruiting NCT03586622 - One Year Home Monitoring and Treatment of IBS Patients N/A
Completed NCT05207618 - Utility of the Administration of Chesnut and Quebracho Extract for Irritable Bowel Syndrome Diarrhea Predominant N/A
Not yet recruiting NCT06369753 - Visible Abdominal Distension N/A
Not yet recruiting NCT05157867 - In Vivo Effects of Amylase Trypsin Inhibitors N/A
Not yet recruiting NCT05100719 - The Role of Irritable Bowel Syndrome in Lactose Intolerance (LION) N/A
Recruiting NCT05001997 - Effects of Lactose-free Dairy Products on Athletes With Irritable Bowel Syndrome N/A
Recruiting NCT02953171 - Probiotics in the Treatment of Irritable Bowel Syndrome N/A
Completed NCT02977975 - Lacto-fermented Sauerkraut in the Treatment of Irritable Bowel Syndrome N/A
Completed NCT03266068 - Epidemiology and Pathophysiology of Post-Infectious Functional GI Disorders
Completed NCT03318614 - Bifidobacterium Infantis M-63 Improves Mental Health in Irritable Bowel Syndrome Developed After a Major Flood Disaster Phase 2/Phase 3
Completed NCT02980406 - The Role of FODMAPs in Upper GI Effects, Colonic Motor Activity and Gut-brain Signaling at the Behavioral Level N/A