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Clinical Trial Summary

To assess the efficacy and safety of the early administration of somatostatin in infusion during 72 hours plus 2 boluses, compared to placebo in the control of acute severe UGIB with suspicion of PUB.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double-Blind


Related Conditions & MeSH terms


NCT number NCT00152399
Study type Interventional
Source UCB Pharma
Contact
Status Completed
Phase Phase 2
Start date September 2000
Completion date October 2005

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