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Sponsored by: |
AstraZeneca |
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Information provided by: | AstraZeneca |
ClinicalTrials.gov Identifier: | NCT00318994 |
To measure meropenem pancreatic tissue penetration in subjects with severe pancreatitis requiring surgery between 30 to 60 minutes after a bolus of 1 g IV meropenem given during the induction period of anesthesia.
Condition | Intervention | Phase |
---|---|---|
Pancreatitis |
Drug: Meropenem |
Phase IV |
Study Type: | Interventional |
Study Design: | Treatment, Non-Randomized, Open Label, Dose Comparison, Single Group Assignment, Pharmacokinetics Study |
Official Title: | Evaluation of Pancreatic Tissue Penetration of Meronem® in the Prophylaxis of Septic Complications in Severe Pancreatitis |
Estimated Enrollment: | 6 |
Study Start Date: | February 2002 |
Study Completion Date: | May 2007 |
Primary Completion Date: | September 2005 (Final data collection date for primary outcome measure) |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Study ID Numbers: | 3591/9010, D9211C09010 |
Study First Received: | April 26, 2006 |
Last Updated: | January 11, 2008 |
ClinicalTrials.gov Identifier: | NCT00318994 |
Health Authority: | Colombia: INVIMA Instituto Nacional de Vigilancia de Medicamentos y Alimentos |
Digestive System Diseases Meropenem Pancreatic Diseases Pancreatitis |