Recruiting
Phase 2

REPEL-CV

Sponsor:

SyntheMed

Code:

NCT00116233

Conditions

Adhesions

Eligibility Criteria

Sex: All

Age: 0 - 1

Healthy Volunteers: Not accepted

Interventions

REPEL-CV

Study Details

Brief summary:

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

Conditions

Adhesions

Study ID

NCT00116233

Status verified date

Jun, 2005

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 0 - 1

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Stage sternotomies

Exclusion Criteria:

  • Delayed closure beyond 5 days

Study Design

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Interventions

REPEL-CV

Central Contacts and Locations

Central contacts

Eli Pines, Ph.D.

212-460-9488

Locations

SyntheMed

Recruiting

Little Silver, New Jersey, United States, 07739

Contacts

Eli Pines, Ph.D.

212-460-9488

More Information

Sponsor

SyntheMed

Last update posted

Jun 28, 2005

Last verified

Jun, 2005

Keywords

  • post operative adhesions

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by SyntheMed on 2005-06-28.