- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00124202
Effect of a Fatty Meal on Endoscopic Retrograde Cholangiopancreatography (ERCP)
Effect of a Fatty Meal on Cannulation at Endoscopic Retrograde Cholangiopancreatography
Study Overview
Detailed Description
A fatty meal is a potent stimulator of cholecystikinin (CCK) in human body. The biological effect of CCK is increasing bile secretion and relaxing the sphincter of Oddi. Theoretically, a fatty meal should facilitate the effect on cannulation at ERCP. If a fatty meal can make the major papilla cannulation easier, it may significantly shorten the procedure time for ERCP and even decrease complications of the procedure, since the complication rate of post-ERCP is positively related to the time of the procedure.
Comparison: Approximately one hour before ERCP procedure, patient will have a fatty meal in the study group and normal saline in control group.
Study Type
Enrollment (Actual)
Phase
- Phase 2
- Phase 1
Contacts and Locations
Study Locations
-
-
Georgia
-
Atlanta, Georgia, United States, 30322
- Emory University School of Medicine; Emory University Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Patients, 18 years and older, who are scheduled for ERCP at Emory University Hospital and signed consent before the procedure.
Exclusion Criteria:
- Patients with a known allergy to milk or those who choose not to sign the consent.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Placebo Comparator: a fatty meal vs normal saline
Approximately one hour before ERCP procedure, patient will have a fatty meal in the study group and normal saline in control group
|
Approximately one hour before ERCP procedure, patient will have a fatty meal in the study group and normal saline in control group
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
a fatty meal in the study group and normal saline in control group
Time Frame: the procedure time for ERCP
|
the procedure time for ERCP
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
follow up within 3 days for complication with relation to the cannulation time
Time Frame: within 3 days
|
within 3 days
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 229-2003
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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