Multicentre randomised controlled trial of a self-assembling haemostatic gel to prevent delayed bleeding following endoscopic mucosal resection (PURPLE Trial)
- PMID: 39988360
- DOI: 10.1136/gutjnl-2024-334229
Multicentre randomised controlled trial of a self-assembling haemostatic gel to prevent delayed bleeding following endoscopic mucosal resection (PURPLE Trial)
Abstract
Background: Prophylactic application of a haemostatic gel to the resection field may be an easy way to prevent delayed bleeding, a frequent complication after endoscopic mucosal resection (EMR).
Objective: We aimed to evaluate if the prophylactic application of a haemostatic gel to the resection field directly after EMR can reduce the rate of clinically significant delayed bleeding events.
Design: We conducted a prospective randomised trial of patients undergoing hot-snare EMR of flat lesions in the duodenum (≥10 mm) and colorectum (≥20 mm) at 15 German centres. Prophylactic clip closure was not allowed, but selective clipping or coagulation could be used prior to randomisation to treat intraprocedural bleeding or for prophylactic closure of visible vessels. Patients were randomised to haemostatic gel application or no prophylaxis. The primary endpoint was delayed bleeding within 30 days.
Results: The trial was stopped early due to futility after an interim analysis. The primary endpoint was analysed in 232 patients (208 colorectal, 26 duodenal). Both groups were comparable in age, sex, comorbidities and lesion characteristics. Preventive measures, such as selective clipping or coagulation, were applied prior to randomisation in 51.9% of cases, with no difference between groups. Delayed bleeding occurred in 14 cases (11.7%; 95% CI 7.1% to 18.6%) after Purastat and in 7 cases (6.3%; 95% CI 3.1% to 12.3%) in the control group (p=0.227), with no difference between colorectal and duodenal subgroups.
Conclusion: The application of a haemostatic gel following EMR of large flat lesions in the duodenum and colorectum does not reduce the rate of delayed bleeding.
Keywords: BLEEDING; CLINICAL TRIALS; COLORECTAL ADENOMAS; ENDOSCOPIC POLYPECTOMY.
© Author(s) (or their employer(s)) 2025. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ Group.
Conflict of interest statement
Competing interests: In line with the ICMJE Disclosure Form, the authors report the following conflicts of interest:TVH reports lecture fees from Cook Medical, Falk Foundation and 3-D Matrix, research support from 3-D Matrix, and advisory fees from Olympus. NG reports research grants and support from Boston Scientific, Medtronic, and Abbott. JS reports lecture fees from Falk Foundation. TJW received lecture fees and/or travel support from Fujifilm, Boston Scientific, ERBE, Microtech Europe, and the Falk Foundation. DRQ received honoraria for lectures, presentations and educational events by Eli Lilly & Co. and Novo Nordisk and has received support for attending meetings and/or travel from Eli Lilly & Co. and Cook Medical. OM reports lecture fees from 3-D matrix. AK reports lecture fees from Falk Foundation, Ovesco Endoscopy, Olympus and advisory fees from KLS Martin. All other authors declare no competing interests with relevance to this study.
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