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Pediatric Multicenter Study of REPEL-CV

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00116233
Recruitment Status : Unknown
Verified June 2005 by SyntheMed.
Recruitment status was:  Recruiting
First Posted : June 28, 2005
Last Update Posted : June 28, 2005
Information provided by:

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

Condition or disease Intervention/treatment Phase
Adhesions Device: REPEL-CV Phase 2

Detailed Description:
- Efficacy at second sternotomy

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Study Type : Interventional  (Clinical Trial)
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single
Primary Purpose: Treatment
Official Title: Peds. Multicenter Study

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Adhesions

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

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Ages Eligible for Study:   up to 1 Year   (Child)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Stage sternotomies

Exclusion Criteria:

  • Delayed closure beyond 5 days

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00116233

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Contact: Eli Pines, Ph.D. 212-460-9488

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United States, New Jersey
SyntheMed Recruiting
Little Silver, New Jersey, United States, 07739
Contact: Eli Pines, Ph.D.    212-460-9488      
Sponsors and Collaborators
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Study Director: Eli Pines SyntheMed
Layout table for additonal information Identifier: NCT00116233    
Other Study ID Numbers: LMS0104RCV
First Posted: June 28, 2005    Key Record Dates
Last Update Posted: June 28, 2005
Last Verified: June 2005
Keywords provided by SyntheMed:
post operative adhesions
Additional relevant MeSH terms:
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Tissue Adhesions
Pathologic Processes