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Pediatric Multicenter Study of REPEL-CV

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified June 2005 by SyntheMed.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT00116233
First Posted: June 28, 2005
Last Update Posted: December 9, 2005
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.
Information provided by:
SyntheMed
  Purpose
This trial will study REPEL-CV for reducing post operative adhesions following cardiovascular (cv) surgery.

Condition Intervention Phase
Adhesions Device: REPEL-CV Phase 2

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

Resource links provided by NLM:


Further study details as provided by SyntheMed:

Detailed Description:
- Efficacy at second sternotomy
  Eligibility

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.


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

Inclusion Criteria:

  • Stage sternotomies

Exclusion Criteria:

  • Delayed closure beyond 5 days
  Contacts and Locations
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 ClinicalTrials.gov identifier (NCT number): NCT00116233


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

Locations
United States, New Jersey
SyntheMed Recruiting
Little Silver, New Jersey, United States, 07739
Contact: Eli Pines, Ph.D.    212-460-9488      
Sponsors and Collaborators
SyntheMed
Investigators
Study Director: Eli Pines SyntheMed
  More Information

ClinicalTrials.gov Identifier: NCT00116233     History of Changes
Other Study ID Numbers: LMS0104RCV
First Submitted: June 27, 2005
First Posted: June 28, 2005
Last Update Posted: December 9, 2005
Last Verified: June 2005

Keywords provided by SyntheMed:
post operative adhesions

Additional relevant MeSH terms:
Tissue Adhesions
Cicatrix
Fibrosis
Pathologic Processes