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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04192825
Other study ID # 35RC18_8808_3T-LAP
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 3, 2020
Est. completion date August 3, 2028

Study information

Verified date April 2023
Source Rennes University Hospital
Contact kristell COAT
Phone 299282555
Email kristell.coat@chu-rennes.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Determine the optimal therapeutic combination associated with complete clinical and anatomical remission of anal suppurations of Crohn's disease at 12 months.


Description:

The management of anoperineal suppurations of Crohn's disease is most often based on clinical practice recommendations, the results of randomized controlled trials and also the analysis of monocentric cohort studies from expert centres. In these latter studies, there is an overall improvement in patients during follow-up with a high level of satisfaction (two thirds of cases), often assessed by the operator himself or the clinician who provides therapeutic management. The most striking finding is the one that highlights the use of combined therapeutic strategies combining immunosuppressants, biotherapies, antibiotics, surgical drainage and surgical reconstruction procedures to varying degrees. Thus, the absence of fistula pathway flow in the long term is the consequence of both maintenance treatment with biotherapies and several surgical procedures. When the characteristics of fistula pathways considered healed on clinical examination are analysed by MRI exploration, an active unhealed pathway persists in two thirds of cases, again emphasizing the inadequacy of clinical examination as a means of assessing recovery. For this reason, fistula pathway closure strategies do not provide much greater benefit than simple removal of the drainage loop. Conversely, medical treatment optimization strategies based on MRI evaluation of the therapeutic response have demonstrated high efficacy. It is necessary to (re)define the therapeutic management of patients with anoperineal lesions. This strategy must be based on a better initial stratification of patients based on prognostic factors derived from available scientific data. A second step consists in setting therapeutic efficacy objectives that take into account the control of the inflammatory component of anal Crohn's disease and the preservation of the anatomical and functional capital of the anus. Only a large prospective cohort at the national level provides the opportunity to study these prognostic factors and to specify the level of optimal therapeutic responses


Recruitment information / eligibility

Status Recruiting
Enrollment 440
Est. completion date August 3, 2028
Est. primary completion date August 3, 2025
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Persons over 18 years of age - People suffering from anal suppuration of Crohn's disease for whom a drainage procedure is planned. - Person who has received written and oral information about the protocol and has not expressed opposition to participate in the study. Exclusion Criteria: - No one who is unable to have an anesthetic, structural or psychological examination by MRI and/or surgery. - Person planning a planned absence that could hinder participation in the research (travel abroad, relocation, impending transfer); - Person with an associated pathology that is a priority for care; - Vulnerable person (minors, persons under guardianship or curatorship, or deprived of their liberty by a judicial or administrative decision

Study Design


Intervention

Procedure:
surgical treatment
surgical drainage and/or surgical reconstruction procedures to anoperineal suppurations according to the doctor's decision

Locations

Country Name City State
France Centre Hospitalier de Rennes Rennes

Sponsors (1)

Lead Sponsor Collaborator
Rennes University Hospital

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical and anatomical healing The healing of anal fistula is defined by the combination of two criteria at 12 months :
MRI criteria = absence of a T2 hyper signal from the path(s) AND the absence of an abscess AND
Complete clinical response = no pain, no discharge, and no drain
12 months.
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