# Effect of a self-assembling peptide hydrogel on delayed bleeding following endoscopic sphincterotomy: Prospective pilot cohort study

**Authors:** Yusuke Ishida, Naoaki Tsuchiya, Takehiko Koga, Takanori Kitaguchi, Keisuke Matsumoto, Makoto Fukuyama, Kaori Hata, Kei Nishioka, Noriko Shiga, Tsutomu Iwasa, Hiroto Ishikawa, Ryohei Nomaru, So Imakiire, Hiroki Matsuoka, Nobuaki Kuno, Sadahiro Funakoshi, Shinya Ashizuka, Eiji Sadashima, Fumihito Hirai

PMC · DOI: 10.1055/a-2803-3921 · Endoscopy International Open · 2026-02-25

## TL;DR

A new self-assembling peptide hydrogel may help control bleeding after a common endoscopic procedure, with promising initial results.

## Contribution

This is the first prospective pilot study evaluating a self-assembling peptide hydrogel for managing delayed bleeding after endoscopic sphincterotomy.

## Key findings

- 26 out of 27 patients in the SAPH group achieved successful hemostasis using the hydrogel alone.
- No delayed bleeding occurred in the SAPH group, while 1.57% of the control group experienced delayed bleeding.
- The hydrogel showed no significant adverse events and similar outcomes after propensity score matching.

## Abstract

Endoscopic sphincterotomy (EST) is important in endoscopic retrograde cholangiopancreatography, but bleeding remains its common complication. This pilot study evaluated the efficacy and safety of a self-assembling peptide hydrogel (SAPH; PuraStat) in managing EST-related hemorrhage.

A prospective cohort study was conducted from June 2023 to March 2024 at three hospitals in Japan, enrolling patients undergoing EST. Patients were divided into SAPH (received SAPH for EST-related bleeding) and control groups (patients without EST-related hemorrhage); primary endpoint was incidence of delayed bleeding.

Of the 254 patients analyzed, 27 were in the SAPH group and 227 in the control group. Background factors related to bleeding were aligned using propensity score matching (PSM). Incidence of EST-related bleeding was 10.6% (27/254). In the SAPH group, 26 of 27 patients (96.3%) achieved successful hemostasis using SAPH alone. Although no delayed bleeding occurred in this group, it occurred in four patients in the control group (1.57%, 4/254). Other adverse events showed no significant difference between the groups. Results were similar to those after PSM and in the subgroup analysis excluding those with self-expandable metallic stent placement.

SAPH is a simple, effective, and safe hemostatic option for treating EST-related hemorrhage and may be a promising first-line approach. This pilot study did not demonstrate a significant reduction in delayed bleeding, but absence of delayed bleeding in the SAPH group is noteworthy and suggests a potential preventive benefit. Thus, larger randomized controlled trials are warranted to validate these preliminary findings.

## Full-text entities

- **Diseases:** cholangitis (MESH:D002761), duodenal stricture (MESH:D003251), periampullary diverticulum (MESH:D004240), Bleeding (MESH:D006470), liver cirrhosis (MESH:D008103), acute pancreatitis (MESH:D010195), malignant biliary obstruction (MESH:D009369), gastrointestinal bleeding (MESH:D006471), EPBD (MESH:D002291), gastrointestinal tract bleeding (MESH:D005770), stone (MESH:D007669), AEs (MESH:D064420), balloon dilation (MESH:D002311), gastrointestinal hemostases (MESH:D005767), SAPH (MESH:C564991)
- **Chemicals:** epinephrine (MESH:D004837), SAPH (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** Q290V

## Full text

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## Figures

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## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12951035/full.md

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Source: https://tomesphere.com/paper/PMC12951035