Adhesions Clinical Trial
Official title:
Peds. Multicenter Study
NCT number | NCT00116233 |
Other study ID # | LMS0104RCV |
Secondary ID | |
Status | Recruiting |
Phase | Phase 2 |
First received | June 27, 2005 |
Last updated | June 27, 2005 |
This trial will study REPEL-CV for reducing post operative adhesions following cardiovascular (cv) surgery.
Status | Recruiting |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A to 1 Year |
Eligibility |
Inclusion Criteria: - Stage sternotomies Exclusion Criteria: - Delayed closure beyond 5 days |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | SyntheMed | Little Silver | New Jersey |
Lead Sponsor | Collaborator |
---|---|
SyntheMed |
United States,
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