biliary tract disease
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The study group included patients who required cholangiography. Patients who are planned ERCP. Patients or their family who fully understand and are willing to give a written informed consent about participation.
Exclusion criteria
Exclusion criteria: age 20 years younger; severe heart disease; severe lung disease; prostatic hyperplasia; glaucoma; contraindication to scopolamine butylbromide; pregnant and breast-feeding women or women suspected of being pregnant; women are not willing to avoid pregnancy during the duration of study; acute pancreatitis; chronic pancreatitis with an acute exacerbation; post gastrectomy; biliary cannulation using with Rendezvous method; contrast medium allergy; or refusal to provide informed consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome was the rate of peristalsis suppression of duodenum after treatment. | — |
Countries
Japan
Contacts
Kyoto prefectural Yosanoumi hospital Department of gastroenterology and hepatology