Prevention of Post-sphincterotomy Bleeding
Recruiting
N/A
Interventional Study
Post-ERCP Bleeding
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 95
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 120 (estimated)
- Sponsor
- National Cheng-Kung University Hospital · Other
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About This Trial
Background and Aim: Endoscopic retrograde cholangiopancreatography (ERCP) and sphincterotomy (EST) are standard treatments for choledocholithiasis. However, 10% of post-EST bleeding was reported. Currently, there are no effective methods or medications for the prevention of post-EST bleeding. This study aimed to investigate whether the local administration of TXA and sucralfate can reduce the post…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patients aged ≥ 18 years who accept ERCP and sphincterotomy for common bile duct (CBD) stone extraction
Exclusion Criteria:
* Paitnets with no schedules for sphincterotomy
* Paitnets with unsuccessful CBD cannulation
* Patients with allergy to sucralfate
Contacts