A Comparison of Monosyn and Monocryl Sutures in Surgical Wounds

CompletedOBSERVATIONAL
Enrollment

48

Participants

Timeline

Start Date

July 31, 2007

Primary Completion Date

March 31, 2008

Study Completion Date

March 31, 2008

Conditions
Wounds
Interventions
OTHER

Absorable, monofilament sutures: Monosyn and Monocryl

Subjects were randomized to Monosyn vs. Monocryl suture arms. The designated skin lesion was removed surgically. The surgical repair of the defect was performed by dividing the wound in half by a single Prolene suture. The appropriate suture was opened by the Study Coordinator and passed sterilely to the surgical technician. The surgical technician loaded the suture, and passed it in a blinded fashion to the physician who closed the appropriate half of the surgical defect. One half of the wound was closed with one suture and the other half was closed with the other suture. Each patient served as their own control, as both sutures were used in each study patient.

Trial Locations (1)

02111

Tufts Medical Center, Boston

All Listed Sponsors
lead

Tufts Medical Center

OTHER

NCT00731913 - A Comparison of Monosyn and Monocryl Sutures in Surgical Wounds | Biotech Hunter | Biotech Hunter