The impact of two type of guidewire for passing of biliary stricture during endoscopic retrograde cholangiopancreatography : a randomized controlled trial

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CRIS

Registry ID

KCT0003510

Enrollment

170

Registered

2019-02-15

Start date

2019-03-04

Completion date

Unknown

Last updated

2019-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Medical Device : After the endoscopy is placed in the duodenum, cannulation is performed on the bile duct using selective cannulation using the method preferred by the endoscopist. Conventional wire a

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients with suspect or exist biliary tract disease in the liver patients are requiring ERCP for treatment or diagnosis Patients who need to be treated with guidewire during the procedure Patients with benign or malignant stricture of the biliary system in CT or MR examination

Exclusion criteria

Exclusion criteria: Under 18 year old A pregnant patient Patients who had hypersensitivity of contrast agents Patients who have difficulty in accessing the ampulla due to previously abdominal surgery (total gastrectomy, total gastrectomy, etc.) Failure of selective cannulation of bile duct Distal common bile duct sticture

Design outcomes

Primary

Measure	Time frame
Successful procedure time (stricture passing time)	—

Secondary

Measure	Time frame
Success rate (stricture passing rate)	—

Countries

Korea, Republic of

Contacts

Public ContactSung Yong Han

Pusan National University Hospital

mirsaint@hanmail.net+82-51-240-7869

Outcome results