DuraSeal Sealant Post Market Study

NACompletedINTERVENTIONAL
Enrollment

237

Participants

Timeline

Start Date

September 30, 2005

Primary Completion Date

May 31, 2009

Study Completion Date

May 31, 2009

Conditions
Elective Cranial Procedures With Dural Incision
Interventions
DEVICE

DuraSeal Dural Sealant System

The DuraSeal™ Dural Sealant System is a polyethylene glycol (PEG) hydrogel that has been FDA approved as a dural sealant to achieve watertight dural closure in cranial and spinal surgery after primary repair with suturing is complete. It was developed as a means of providing a dural seal by covering small holes around the suture with an absorbable hydrogel. DuraSeal should only be used with autologous duraplasty material.

OTHER

Standard of Care

Standard procedure to obtain intraoperative watertight dural closure. These methods could have included additional sutures, adhesive glue, absorbable gelatin sponge, dural substitute, soft tissue patch, or another method typically used by the investigator.

Trial Locations (1)

02451

Confluent Surgical, Waltham

Sponsors
All Listed Sponsors
collaborator

Medtronic - MITG

INDUSTRY

lead

Integra LifeSciences Corporation

INDUSTRY

NCT00704340 - DuraSeal Sealant Post Market Study | Biotech Hunter | Biotech Hunter