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| Sponsored by: |
Schering-Plough |
| Information provided by: | Schering-Plough |
| ClinicalTrials.gov Identifier: | NCT00040131 |
Purpose
The purpose of this study is to determine if a single dose of IL-10 compared to placebo is safe and effective in reducing the incidence of post-ERCP acute pancreatitis for subjects with increased risk.
| Condition | Intervention | Phase |
|
Bile Duct Diseases Biliary Tract Diseases Gallbladder Diseases Pancreatitis Pancreatic Diseases |
Drug: IL-10 |
Phase II |
| MedlinePlus related topics: | Gallbladder Diseases Pancreatic Diseases |
| Study Type: | Interventional |
| Study Design: | Prevention, Randomized, Double-Blind, Placebo Control, Single Group Assignment, Safety/Efficacy Study |
Eligibility
| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion criteria:
Adults weighing up to 125 kg who are undergoing ERCP for any of the following:
Exclusion criteria:
Contacts and Locations
More Information
| Study ID Numbers: | P02580 |
| First Received: | June 20, 2002 |
| Last Updated: | May 31, 2006 |
| ClinicalTrials.gov Identifier: | NCT00040131 |
| Health Authority: | United States: Food and Drug Administration |
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