DuraGen Plus® Adhesion Barrier for Use in Spinal Surgery

Status Terminated

Clinical Trial Summary

To evaluate the safety and effectiveness of DuraGen Plus® Adhesion Barrier Matrix as an adhesion barrier in spinal surgery to reduce the extent of peridural fibrosis formation and radicular pain in comparison to a control group receiving standard care.

Clinical Trial Description

For more information, please visit www.DuragenStudy.com ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00387829
Study type	Interventional
Source	Integra LifeSciences Corporation
Contact
Status	Terminated
Phase	N/A
Start date	October 2006
Completion date	December 2011

View Details

See also
Status	Clinical Trial	Phase
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
Recruiting	`NCT00116233` - Pediatric Multicenter Study of REPEL-CV	Phase 2