Actively Recruiting
Prevention of Post-sphincterotomy Bleeding
Led by National Cheng-Kung University Hospital · Updated on 2025-05-25
120
Participants Needed
1
Research Sites
82 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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-EST bleeding event. Methods: This is a randomized clinical trial. Patients with choledocholithiasis scheduled for ERCP with EST at National Cheng Kung University Hospital and Siriraj Hospital were enrolled. The study will recruit 120 patients. After randomization, 60 patients will be classified into the intervention group and 60 into the control group. The participants will receive standard ERCP and EST for common bile duct stone removal. If immediate polypectomy bleeding occurs, the investigators will apply standard endoscopic therapy by either local injection of diluted epinephrine or heater probe coagulation. After then, the investigators will spray 2g of sucralfate powder and 1g of tranexamic acid through duodenoscopy precisely on the post-EST wound in the intervention group. All enrolled patients will be monitored for delayed bleeding for 14 days after the ERCP.
CONDITIONS
Official Title
Prevention of Post-sphincterotomy Bleeding
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 60; 18 years who accept ERCP and sphincterotomy for common bile duct (CBD) stone extraction
You will not qualify if you...
- Patients not scheduled for sphincterotomy
- Patients with unsuccessful common bile duct cannulation
- Patients allergic to sucralfate
AI-Screening
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Trial Site Locations
Total: 1 location
1
National Cheng-Kung University Hospital
Tainan, Other (Non U.s.), Taiwan, 704
Actively Recruiting
Research Team
H
Hsueh-Chien Chiang, M.D.
CONTACT
X
Xi-Zhang Lin, M.D.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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