Pediatric Multicenter Study of REPEL-CV
NCT00116233 · Status: UNKNOWN · Phase: PHASE2 · Type: INTERVENTIONAL
Last updated 2005-06-28
Summary
This trial will study REPEL-CV for reducing post operative adhesions following cardiovascular (cv) surgery.
Conditions
- Adhesions
Interventions
- DEVICE
-
REPEL-CV
Sponsors & Collaborators
-
SyntheMed
lead INDUSTRY
Principal Investigators
-
Eli Pines · SyntheMed
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 1 Day
- Max Age
- 1 Year
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
Countries
- United States
Study Locations
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