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Pediatric Multicenter Study of REPEL-CV

Peds. Multicenter Study

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00116233
Enrollment
Unknown
Registered
2005-06-28
Start date
Unknown
Completion date
Unknown
Last updated
2005-06-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adhesions

Keywords

post operative adhesions

Brief summary

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

Detailed description

\- Efficacy at second sternotomy

Interventions

DEVICEREPEL-CV

Sponsors

SyntheMed
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE

Eligibility

Sex/Gender
ALL
Age
1 Days to 1 Years
Healthy volunteers
No

Inclusion criteria

* Stage sternotomies

Exclusion criteria

* Delayed closure beyond 5 days

Countries

United States

Contacts

Primary ContactEli Pines, Ph.D.
212-460-9488

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026