RecruitingPhase 2NCT04010526

Evaluation of Local Co-administration of Autologous ADIpose Derived Stromal Vascular Fraction With Microfat for Refractory Perianal CROHN's Fistulas.

Double-blind Randomised Placebo Controlled Study Evaluating Local Co-administration of Autologous ADIpose Derived Stromal Vascular Fraction With Microfat for Refractory Perianal CROHN's Fistulas.


Sponsor

Assistance Publique Hopitaux De Marseille

Enrollment

84 participants

Start Date

Feb 19, 2020

Study Type

INTERVENTIONAL

Conditions

Summary

Autologous ADSVF constitutes an innovative therapeutic strategy that concentrates various types of regenerative stem cells and paracrine factors able to promote angiogenesis and tissue repair. Together with the ease of collection from a minimally manipulated lipoaspirate, the unique properties of ADSVF offer new opportunities for fistulas' healing in patients with CD. The use of ADSVF is currently developed in many clinical fields based on safety and efficacy data. Our ADICROHN pilot study evaluating safety and tolerance of local administration of autologous ADSVF with microfat in CD patients with complex perianal fistula refractory to conventional medical and surgical therapy showed that this novel therapeutic approach appears feasible and safe. However the therapeutic potential of local this combined treatment in healing refractory perianal Crohn's fistulas still remains to be demonstrated. The main objective of this study is to assess the efficacy of local injection of autologous ADSVF and microfat versus placebo for the treatment of complex refractory perianal Crohn's fistulas at week 24. The efficacy will be assessed on clinical assessment of closure of all the external openings that were drained at baseline, and MRI confirmation of absence of collections \> 2 cm of the treated perianal fistulas at week 24.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a new treatment for stubborn anal fistulas in people with Crohn's disease — tunnels that form between the bowel and skin near the anus that are very difficult to heal. The treatment uses fat tissue taken from the patient's own body (adipose-derived stromal vascular fraction and microfat) injected directly into the fistula. **You may be eligible if...** - You have had Crohn's disease for at least 6 months - You have a complex perianal fistula that has not responded to standard treatments - Your Crohn's disease in the gut is inactive or only mildly active - You are 18 or older and in reasonable general health - Women of childbearing age must have a negative pregnancy test and agree to use contraception **You may NOT be eligible if...** - Your gut Crohn's disease is significantly active - You have an active infection in the fistula area that is not controlled - You have other serious medical conditions that would make the procedure unsafe - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

COMBINATION_PRODUCTlocal co-administration of autologous ADIpose

local co-administration of autologous ADIpose derived stromal vascular fraction and microfat for refractory perianal CROHN's fistulas Each batch of the final product is composed of one 5 mL syringes containing 25,9 +/- 10,7 millions viable cells. Each syringe will be obstructed with a sterile stopper and packaged in an external packaging.

OTHERplacebo

local co-administration of placebo The study placebo will consist of a saline solution for intralesional administration and will follow the same administration schema described for the SFV


Locations(1)

Assistance Publique Des Hopitaux de Marseille

Marseille, PACA, France

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NCT04010526


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