Pinaverium Bromide in Post-cholecystectomy Sphincter of Oddi Dysfunction (NCT02833103) | Clinical Trial Compass
UnknownPhase 4
Pinaverium Bromide in Post-cholecystectomy Sphincter of Oddi Dysfunction
China168 participantsStarted 2016-07
Plain-language summary
Sphincter of Oddi dysfunction (SOD) refers to biliary kinetic abnormality of the sphincter of Oddi (SO), often accompanied by pain, hepatic and pancreatic enzyme elevation, common bile duct (CBD) dilation or onset of pancreatitis. Pain caused by SOD affects the quality of life (QoL).The primary objective of this trial is to evaluate the efficacy of relieving abdominal pain of Pinaverium Bromide in medication therapy for patients with post-cholecystectomy SOD.
Who can participate
Age range18 Years – 69 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Chief complaint of upper right abdominal pain following LC (within 2 weeks to 6 months) at a hospital visit, but not a pain caused by surgical incision, lasting 3 to 5 minutes each time, without a history of other biliary tract operation
* No presence of intestinal obstruction as evidenced by plain abdominal X-ray, with peptic ulcer and duodenal diverticulum ruled out through barium meal examination or gastroscopy
* No other obvious abnormalities as evidenced by abdominal ultrasound B and MRCP, except for bile duct dilation
* Patients with biliary-type sphincter of Oddi dysfunction (SOD) who are classified as SOD type II (biliary-type abdominal pain accompanied by hepatic enzyme elevation or common bile duct (CBD) dilation) and SOD type III (only biliary-type abdominal pain) according to Geenen-Hogan classification criteria
Exclusion Criteria:
* Postoperative biliary calculi, benign biliary stenosis, bile duct infection, overlong residual cystic duct (\> 0.5cm), biliary tumors, etc.
* Peptic ulcer, duodenal diverticulum
* Pancreatitis, pancreatic-type SOD
* Adhesive intestinal obstruction
* Postoperative irritable bowel syndrome (IBS)
* A history of abdominal operation or other surgery
* Pregnant and lactating women
* Use of other drugs from one week after LC to enrollment, including antispasmodic drugs, analgesics, choleretic agents, calcium ion antagonists and GI motility drugs
* A history of allergy to Pinaverium Bromide / Danshu Tablets
What they're measuring
1
Efficacy Evaluation of Reduction in Abdominal Pain Scores,Change From Baseline to 3 Months After Medication
Timeframe: Change From Baseline to 3 Months After Medication
Trial details
NCT IDNCT02833103
SponsorXinhua Hospital, Shanghai Jiao Tong University School of Medicine