common bile duct stone
Conditions
Interventions
Groups using conventional standard protocol (7.5 fps, Mid)
Groups using new CE protocol (3.75fps, Low)
Sponsors
Keio University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: The subjects of this study are patients over 18 years old who will undergo the following ERCP treatments at Keio University Hospital and who have given their consent. 1) Patients undergoing initial stone removal for common bile duct stones 2) Patients who undergo first stone removal after bile duct stenting for acute cholangitis
Exclusion criteria
Exclusion criteria: 1) Those under 18 years of age 2) BMI over 30 3) Pregnant or suspected pregnancy 4) If the patient is unable to give consent 5) If it is difficult to obtain consent from the subject of the research due to a disturbance in consciousness, cognitive dysfunction, or mental retardation at the time of obtaining consent 6) Other cases in which the person in charge deems it inappropriate for the subject to participate in this research
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Radiation dose in ERCP | — |
Secondary
| Measure | Time frame |
|---|---|
| Clinical success rate of treatment and exposure time | — |
Countries
Japan
Contacts
Public ContactTakaoki Hayakawa
Keio University School of Medicine Division of Gastroenterology and Hepatology, Department of Internal Medicine
Outcome results
None listed