Regenerative Endoscopy in Refractory Perianal Crohn's Disease

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorAsian Institute of Gastroenterology, India

About this trial

Perianal fistulizing Crohn's disease (pCD) represents a severe phenotype of Crohn's disease, affecting approximately 20-30% of patients and resulting in chronic drainage, recurrent sepsis, impaired continence, and reduced quality of life. Despite optimization of biologics, antibiotics, and surgical drainage, durable healing remains difficult to achieve. Conventional surgical approaches such as curettage or seton management alone yield modest remission rates, and repeated procedures may compromise sphincter integrity.

Autologous mechanically processed tissue stromal vascular fraction (tSVF) is derived from adipose tissue using non enzymatic methods and can be prepared and reinjected during the same operative session. Unlike culture-expanded or enzymatically isolated cell products, mechanical tSVF retains a native adipose micro architecture containing stromal cells, perivascular elements, endothelial progenitors, extracellular matrix components, and bioactive cytokines. This heterogeneous microenvironment is hypothesized to exert immunomodulatory, pro angiogenic, and regenerative effects that may enhance tract healing while preserving sphincter function.

Mechanical processing avoids enzymatic digestion, cell expansion, and complex laboratory infrastructure, making it potentially more feasible and cost effective in real world settings. However, high quality prospective data evaluating mechanically processed autologous tSVF specifically in refractory complex pCD remain limited, and feasibility data are required before undertaking a large randomized trial.

This single arm pilot feasibility study is therefore designed to evaluate procedural feasibility, safety, and preliminary signals of clinical and radiological healing following mechanical tSVF injection in refractory complex perianal Crohn's disease. The results will inform design parameters, outcome variability, and sample size estimation for a future definitive multicenter trial.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age 18-65 years

Crohn's disease with complex perianal fistula (≥1 secondary tract or internal opening involvement)

Refractory to ≥1 biologic and/or ≥1 prior sphincter sparing procedure

No abscess on screening MRI

Disqualifiers

Rectovaginal fistula

Severe active proctitis requiring urgent escalation

Malignancy in tract or pelvic region

Pregnancy or lactation

Trial design

Design model

Single group

Treatments tested in this trial

  • Autologous Mechanical Tissue Stromal Vascular Fraction (tSVF) Injection

    Procedure/Surgery

    Autologous adipose tissue harvest by tumescent liposuction followed by same-session mechanical processing to obtain tissue stromal vascular fraction (tSVF) and local injection into the perianal fistula tract and internal opening region

Treatment groups

50 Participants
are divided into 1 treatment group
Group A: Autologous tSVF Injection for Perianal Crohn's DiseaseExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Feasibility and Preliminary Efficacy at Week 24

•Assess feasibility (recruitment rate, retention to Week 24, protocol adherence, and tSVF processing success rate) and generate preliminary efficacy estimates for mechanical tSVF injection in refractory complex pCD.

Time frame
Week 24

Secondary outcomes

1

Cessation of fistula drainage

* Time to cessation of drainage * Change in Perianal Disease Activity Index (PDAI) from baseline * MRI tract volume and signal intensity changes (quantified centrally) * Vaizey continence score change * Short Inflammatory Bowel Disease Questionnaire (SIBDQ) change * Recurrence and fistula related interventions * Safety: procedure related and systemic adverse events

Time frame
Week 24 & 52

Other outcomes

Sponsors and contacts

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