NCT02770495

Brief Summary

It is assumed that gut inflammation and lesions characterizing flares of Crohn's disease (CD) result from an aberrant T-cell mediated immune responses characterized by a complex balance between peripheral and lamina propria regulatory and effector T cell subsets. Because most of CD patients who undergo a surgery experienced a postoperative endoscopic recurrence of the disease (70 % at one year) leading to a clinical recurrence (10 % per year), the "model" of postoperative recurrence in CD represents a privileged situation that mimicks what happens in the gut of CD patients in clinical remission before the occurrence of further flares. It is likely that the same factors which underlie the immunopathogenesis of CD at its early stages also contribute to disease recurrence in the postoperative setting. Indeed, the postoperative state is performed for intent of disease remission and this situation represents probably an ideal setting to investigate the dynamics of most of T cell subsets in the peripheral and mucosal compartments because one may argue that removal of the diseased segment of bowel resets the disease to its earliest phases, providing an interesting window to better understand which T cell subsets predispose to disease recurrence. That is the reason why this model will be used in the present project i) to understand better the immunopathogenesis of CD relapse; ii) to identify novel and promising immune cell-associated biomarkers capable to predict relapse of the disease and finally iii) to identify potential specific therapeutic target associated with T cell subsets involved in the initiation of disease.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
59

participants targeted

Target at below P25 for phase_3

Timeline
Completed

Started Jan 2011

Longer than P75 for phase_3

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2011

Completed
5.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2016

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

May 9, 2016

Completed
3 days until next milestone

First Posted

Study publicly available on registry

May 12, 2016

Completed
Last Updated

December 4, 2025

Status Verified

November 1, 2025

Enrollment Period

5.3 years

First QC Date

May 9, 2016

Last Update Submit

November 27, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Postoperative endoscopic recurrence, assessed by a Rutgeerts 's score > i1, over the one-year post-surgery follow-up

    Rutgeerts 's score \> i1

    at one year

Secondary Outcomes (2)

  • proportion of T cell subsets in the arm of patients who will experience a recurrence and those who will not.

    at 3 months before relapse

  • number of T cell subsets in the arm of patients who will experience a recurrence and those who will not.

    at 3 months before relapse

Study Arms (1)

Postoperative endoscopic recurrence

EXPERIMENTAL

Patients with a diagnosis of Crohn's disease who undergo an ileo-colonic curative resection

Other: blood sample

Interventions

Postoperative endoscopic recurrence

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Aged over 18 years
  • Men or non-pregnant women
  • Patients with a diagnosis of Crohn's disease who undergo an ileo-colonic curative resection
  • No change of the postoperative treatment before assessing an endoscopic recurrence during the one-year post surgery follow-up period
  • Informed consent given

You may not qualify if:

  • Pregnancy
  • History of disease, including mental/emotional disorder, that might interfere with their participation in the study
  • Inability to comply with the protocol requirements
  • Inability to fill in the diary cards

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Service d'Hépato-Gastroentérologie Centre hospitalier Lyon Sud Hospices Civils de Lyon

Pierre-Bénite, France

Location

Related Publications (1)

  • Boschetti G, Nancey S, Moussata D, Cotte E, Francois Y, Flourie B, Kaiserlian D. Enrichment of Circulating and Mucosal Cytotoxic CD8+ T Cells Is Associated with Postoperative Endoscopic Recurrence in Patients with Crohn's Disease. J Crohns Colitis. 2016 Mar;10(3):338-45. doi: 10.1093/ecco-jcc/jjv211. Epub 2015 Nov 19.

MeSH Terms

Conditions

Crohn Disease

Interventions

Blood Specimen Collection

Condition Hierarchy (Ancestors)

Inflammatory Bowel DiseasesGastroenteritisGastrointestinal DiseasesDigestive System DiseasesIntestinal Diseases

Intervention Hierarchy (Ancestors)

Specimen HandlingClinical Laboratory TechniquesDiagnostic Techniques and ProceduresDiagnosisPuncturesSurgical Procedures, OperativeInvestigative Techniques

Study Officials

  • Stéphane NANCEY, MD

    Service d'Hépato-Gastroentérologie Centre hospitalier Lyon Sud Hospices Civils de Lyon

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
phase 3
Allocation
NA
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 9, 2016

First Posted

May 12, 2016

Study Start

January 1, 2011

Primary Completion

April 1, 2016

Study Completion

April 1, 2016

Last Updated

December 4, 2025

Record last verified: 2025-11

Locations