Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00116233
Other study ID # LMS0104RCV
Secondary ID
Status Recruiting
Phase Phase 2
First received June 27, 2005
Last updated June 27, 2005

Study information

Verified date June 2005
Source SyntheMed
Contact Eli Pines, Ph.D.
Phone 212-460-9488
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

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


Description:

- Efficacy at second sternotomy


Recruitment information / eligibility

Status Recruiting
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group N/A to 1 Year
Eligibility Inclusion Criteria:

- Stage sternotomies

Exclusion Criteria:

- Delayed closure beyond 5 days

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
REPEL-CV


Locations

Country Name City State
United States SyntheMed Little Silver New Jersey

Sponsors (1)

Lead Sponsor Collaborator
SyntheMed

Country where clinical trial is conducted

United States, 

See also
  Status Clinical Trial Phase
Terminated NCT00387829 - DuraGen Plus® Adhesion Barrier for Use in Spinal Surgery N/A
Completed NCT04100447 - A Study to Evaluate the Safety, Tolerability and Efficacy of LB1148 for Subjects Undergoing Elective Bowel Resection Phase 1
Completed NCT01794221 - The Role of 2-octyl Cyanoacrylate in Prevention of Recurrent Adhesions After Circumcision N/A
Completed NCT00565643 - Seprafilm® Adhesion Barrier and Cesarean Delivery Phase 4
Completed NCT01355939 - Comparative Effectiveness Multicenter Trial for Adhesion Characteristics of Ventral Hernia Repair Mesh N/A
Suspended NCT00865488 - Evaluation of Adhexil Safety and Efficacy in Prevention and/or Reduction of Adhesions in Gynecological Surgery Phase 3
Completed NCT00531739 - SurgiWrapTM to Reduce Soft Tissue Attachment & Incidence Early Post-Operative Bowel Obstruction in Colorectal Surgery Phase 4
Completed NCT02166554 - The Efficacy and Safety Study of a New Cross-linked Hyaluronan Hydrogel in the Reduction of Postsurgical Peritoneal Adhesions Phase 1/Phase 2
Completed NCT00530322 - Adhesion Formation Following Laparoscopic and Open Colorectal Surgery N/A
Completed NCT00646412 - A-Part® Gel as Adhesion Prophylaxis After Major Abdominal Surgery Versus a Non-treated Group Phase 1/Phase 2
Completed NCT02844920 - Evaluation of Uterine Patency Following Sonography-guided Transcervical Ablation of Fibroids
Completed NCT01720966 - Adhesions After Open Versus Laparoscopic Resection of Colorectal Malignancies Detected During Liver Resection N/A
Completed NCT00597662 - Safety Study of Polylactide-Caprolactone-Trimethylenecarbonate Copolymer for Post-Operative Adhesion Prophylaxis Phase 1
Completed NCT01183000 - Closure of Peritoneum at Cesarean Section and Postoperative Adhesion N/A
Completed NCT02804139 - Physical Therapy in Addition to Standard Care Following C-Section N/A
Completed NCT00902148 - Evaluation of Bioresorbable Sheet to Prevent Intra-Abdominal Adhesions in Colorectal Surgeries Phase 4
Completed NCT02839564 - Benefit of Laparoscopic Adhesiolysis in Patients With Chronische Abdominal Pain Phase 4