48
Participants
Start Date
July 31, 2007
Primary Completion Date
March 31, 2008
Study Completion Date
March 31, 2008
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.
Tufts Medical Center, Boston
Tufts Medical Center
OTHER