NCT00547638View on ClinicalTrials.gov

Study to Show Equivalence of DERMABOND PROTAPE to DERMABOND HVD for Wound Closure

PHASE2CompletedINTERVENTIONAL
Enrollment

216

Participants

Timeline

Start Date

August 31, 2007

Primary Completion Date

March 31, 2009

Study Completion Date

March 31, 2009

Conditions
Lacerations
Interventions
DEVICE

cyanoacrylate with pressure sensitive mesh

Topical Skin Adhesive

DEVICE

cyanoacrylate

Topical Skin Adhesive

Trial Locations (9)

11794

Stony Brook University HSC, Stony Brook

19102

Drexel University Hospital, Philadelphia

19104

Hospital of the University of Pennsylvania, Philadelphia

27157

Wake Forest University Baptist Medical Center, Winston-Salem

27710

Duke University Health System, Durham

32806

Orlando Regional Healthcare System, Orlando

46268

Investigators Research Group, LLC, Indianapolis

70112

Tulane Universtiy Hospital & Clinic, New Orleans

85016

NextCare Institute For Clinical Research, Phoenix

All Listed Sponsors
lead

Ethicon, Inc.

INDUSTRY

NCT00547638 - Study to Show Equivalence of DERMABOND PROTAPE to DERMABOND HVD for Wound Closure | Biotech Hunter | Biotech Hunter