Now Available for Public Comment: Notice of Proposed Rulemaking (NPRM) for FDAAA 801 and NIH Draft Reporting Policy for NIH-Funded Trials

Pediatric Multicenter Study of REPEL-CV

The recruitment status of this study is unknown because the information has not been verified recently.
Verified June 2005 by SyntheMed.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
SyntheMed
ClinicalTrials.gov Identifier:
NCT00116233
First received: June 27, 2005
Last updated: NA
Last verified: June 2005
History: No changes posted
  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
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind
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

Ages Eligible for Study:   up to 1 Year
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Stage sternotomies

Exclusion Criteria:

  • Delayed closure beyond 5 days
  Contacts and Locations
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, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: 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

No publications provided

ClinicalTrials.gov Identifier: NCT00116233     History of Changes
Other Study ID Numbers: LMS0104RCV
Study First Received: June 27, 2005
Last Updated: June 27, 2005
Health Authority: United States: Food and Drug Administration

Keywords provided by SyntheMed:
post operative adhesions

ClinicalTrials.gov processed this record on November 27, 2014