Pediatric Multicenter Study of REPEL-CV

Status unconfirmed · Phase 2

Conditions studied: Adhesions

In brief

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

Key facts

Study ID

NCT00116233

Run by

SyntheMed

Last updated by the study team

2005-06-28

Who can join

Age: 0 and older, up to 1. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Stage sternotomies

You may not qualify if…

• Delayed closure beyond 5 days

Where it is running

• SyntheMed — Little Silver, New Jersey, United States (enrolling)

Full record on ClinicalTrials.gov

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