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Clinical Trial
. 2025 Sep 9.
doi: 10.1055/a-2665-1777. Online ahead of print.

Regenerative endoscopy for the treatment of difficult gastrointestinal defects: results from a pilot trial

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Clinical Trial

Regenerative endoscopy for the treatment of difficult gastrointestinal defects: results from a pilot trial

Dania Nachira et al. Endoscopy. .

Abstract

Gastrointestinal (GI) defects with inflamed, fibrotic edges are often refractory to traditional endoscopic treatments. This study evaluates the efficacy and safety of endoscopically delivered stromal vascular fraction from autologous adipose tissue (tSVFem), which promotes tissue regeneration in upper and lower GI defects without additional patient risk or cost.This pilot trial involved patients with GI defects accessible by endoscopy after traditional treatments had failed. The tSVFem was derived from harvested hip fat, which was processed and injected endoscopically into the defect margins. The primary outcome was complete defect resolution. Secondary outcomes included treatment frequency, procedure-related adverse events, and recurrence.30 patients were included: 15 with esophageal defects (median diameter 6 mm) and 15 with rectal defects (median diameter 5 mm). Of the 15 esophageal defects, 14 showed complete resolution after tSVFem injection (10 after one injection and 4 after two injections). The overall resolution rate for rectal defects was 60% (six after one treatment, one after two treatments, and two after three or four treatments). The resolution rate was 5/9 for rectal defects communicating with the urinary tract and 4/6 for those communicating with other organs. No intraprocedural or postprocedural adverse events or defect recurrence occurred.These results suggest that endoscopic injection of autologous tSVFem may treat complex esophageal and rectal defects, including those communicating with adjacent organs other than the urinary tract.

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Conflict of interest statement

V. Bove is a consultant for Boston Scientific. C. Spada is a consultant for Medtronic and AnX Robotics, and has received speaker fees from Olympus and Pentax. I. Boskoski is a consultant for Apollo Endosurgery, Boston Scientific, Nitinotes, Pentax, Cook Medical, Microtech, ERBE, Siemens, Myka Labs, and Endo Tools Therapeutics S.A.; conducts sponsored lectures for Apollo Endosurgery, Boston Scientific, Cook Medical, and Microtech; is the recipient of research grants from Apollo Endosurgery, Endo Tool Therapeutics, and ERBE; and is a scientific advisory board member for Nitinotes and Myka labs. The remaining authors declare that they have no conflict of interest.

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