RESTOREGI Study: Regenerative Endoscopic Stromal Therapy: Outcomes and Risk Factor Evaluation in GI Fistulas

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAsian Institute of Gastroenterology, India

About this trial

RESTOREGI Study Benign gastrointestinal fistulas are abnormal communications between the gastrointestinal tract and adjacent organs or the skin. Chronic fistulas are often difficult to treat because of persistent inflammation, fibrosis, impaired vascularity, and defective tissue regeneration. Endoscopic regenerative therapy using mechanically processed autologous total stromal vascular fraction-enriched microfragmented adipose tissue (tSVF-EM) has emerged as a novel therapeutic approach that may promote tissue repair through angiogenesis, immunomodulation, and regenerative signaling.

Although early clinical experience suggests promising healing outcomes, factors predicting successful fistula closure remain poorly understood. The RESTOREGI study is a prospective, single-center observational cohort study designed to identify patient-related, fistula-related, and procedural factors associated with successful healing following endoscopic tSVF-EM therapy in benign gastrointestinal fistulas. The study will also evaluate treatment safety, time to healing, recurrence rates, and the impact of procedural variables on outcomes.

Eligibility criteria

Qualifiers

Age ≥18 years

Confirmed benign gastrointestinal fistula involving the luminal gastrointestinal tract

Fistula accessible for endoscopic evaluation and treatment

Planned treatment with endoscopic tSVF-EM therapy, with or without adjunctive endoscopic therapies (argon plasma coagulation [APC], tract abrasion/curettage, clips, over-the-scope clips [OTSC], endoscopic suturing, or stent placement)

Disqualifiers

Perianal fistulas of any aetiology

Inflammatory bowel disease-associated fistulas, including fistulas related to Crohn's disease or ulcerative colitis

Malignancy-related fistulas

Fistulas requiring primary oncologic surgical management

Trial design

Treatments tested in this trial

  • Endoscopic tSVF-EM Therapy

Treatment groups

50 Participants
are divided into 1 treatment group