NCT00594035View on ClinicalTrials.gov

Study to Evaluate Safety and Effectiveness of Spinal Sealant

NACompletedINTERVENTIONAL
Enrollment

158

Participants

Timeline

Start Date

September 30, 2005

Primary Completion Date

February 29, 2008

Study Completion Date

April 30, 2008

Conditions
Spinal Procedure Requiring Dura Incision
Interventions
DEVICE

Spinal Sealant System

DEVICE

Standard of care

Standard of care: devices intended to provide a watertight closure

Trial Locations (1)

01730

Confluent Surgical, Inc., Bedford

Sponsors
All Listed Sponsors
lead

Integra LifeSciences Corporation

INDUSTRY

NCT00594035 - Study to Evaluate Safety and Effectiveness of Spinal Sealant | Biotech Hunter | Biotech Hunter