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Biliary Dilation Cohort for Association between Opiate Use and Biliary Dilation
N/A
Waitlist Available
Research Sponsored by Stanford University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 3 hours
Awards & highlights
No Placebo-Only Group
Summary
We hope to better define the association between opiate use and biliary dilation, which was evident in our previous retrospective study. This prospective study including all endoscopic ultrasound procedures performed for further evaluation of biliary dilatation in the setting of bilirubin \<2 mg/dL will enable accurate measurement of common bile duct and pancreatic duct diameter using endoscopic ultrasound and identification of other non- obstructive factors which may modulate biliary dilation (i.e. age, cholecystectomy status, duration and type of opiate used).
Eligible Conditions
- Association between Opiate Use and Biliary Dilation
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 3 hours
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 3 hours
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Identification of factors associated with biliary dilation
Identification of factors associated with pancreatic duct dilation
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Biliary Dilation CohortExperimental Treatment1 Intervention
Patients referred for endoscopic evaluation of biliary dilation
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Endoscopic ultrasound
2014
N/A
~140
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Who is running the clinical trial?
Stanford UniversityLead Sponsor
2,472 Previous Clinical Trials
17,501,718 Total Patients Enrolled
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