Pediatric Multicenter Study of REPEL-CV
Peds. Multicenter Study
1 other identifier
interventional
N/A
1 country
1
Brief Summary
This trial will study REPEL-CV for reducing post operative adhesions following cardiovascular (cv) surgery.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 27, 2005
CompletedFirst Posted
Study publicly available on registry
June 28, 2005
CompletedJune 28, 2005
June 1, 2005
June 27, 2005
June 27, 2005
Conditions
Keywords
Interventions
Eligibility Criteria
You may qualify if:
- Stage sternotomies
You may not qualify if:
- Delayed closure beyond 5 days
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- SyntheMedlead
Study Sites (1)
SyntheMed
Little Silver, New Jersey, 07739, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Eli Pines
SyntheMed
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- INDUSTRY
Study Record Dates
First Submitted
June 27, 2005
First Posted
June 28, 2005
Last Updated
June 28, 2005
Record last verified: 2005-06