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Clinical Trial Summary

This trial will study REPEL-CV for reducing post operative adhesions following cardiovascular (cv) surgery.


Clinical Trial Description

- Efficacy at second sternotomy ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00116233
Study type Interventional
Source SyntheMed
Contact Eli Pines, Ph.D.
Phone 212-460-9488
Status Recruiting
Phase Phase 2

See also
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