Haemostatic Gel Prophylaxis for Post Duodenal Endoscopic Resection Bleeding

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorGCS Ramsay Santé pour l'Enseignement et la Recherche

About this trial

The purpose of this study is to test whether prophylactic application of haemostatic gel will reduce the rate of clinically significant bleeding requiring intervention (such as blood transfusion, admission to hospital, other blood products) following endoscopic resection of advanced duodenal neoplasia compared to standard therapy.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Single ampullary lesion ≥ 10mm

Resection via hot ampullectomy, injection/Endoscopic mucosal resection of adjacent lateral spreading component Duodenal Lesions

≤ 2 lesions

Lesion ≥15mm

Disqualifiers

Inability to provide informed consent (including people with cognitive impairment);

Pregnant or breastfeeding women;

Allergy to PuraStat®;

"Cold" mucosal endoscopic resection;

Trial design

Design model

Parallel

Treatments tested in this trial

  • duodenal mucosectomy

    Procedure/Surgery

    Standard resection technique will be performed for duodenal mucosectomy, as well as the usual hemostasis at the discretion of the operator.

  • ampullectomy

    Procedure/Surgery

    Standard resection technique will be performed for ampullectomy, as well as the usual hemostasis at the discretion of the operator.

Treatment groups

234 Participants
are divided into 2 treatment groups
Group A: Experimental Group with PuraStat®Experimental treatment 2 interventions
Group B: Control GroupActive comparator 2 interventions

Trial outcomes

Primary outcomes

1

Bleeding rate requiring further intervention within 30 days

Rate of clinically significant delayed postoperative bleeding requiring further intervention within 30 days (such as blood transfusion, packed cell transfusion or administration of other blood products, hospitalization or repeat endoscopy)

Time frame
30 days

Secondary outcomes

Other outcomes

Sponsors and contacts

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