Clinical Trials Directory

Trials / Terminated

TerminatedNCT00524511

Comparison Study of Wound Closure at Time of Cesarean Delivery: Dermabond Glue Versus Surgical Staples

A Comparative Study of Closure Techniques After Cesarean Section: Staples vs. Dermabond

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
136 (actual)
Sponsor
University of Massachusetts, Worcester · Academic / Other
Sex
Female
Age
Healthy volunteers
Not accepted

Summary

Women who have a cesarean delivery have a surgical incision on their abdomen (belly). The usual way to close this opening is with metal surgical staples. In many other types of surgery, surgical incisions are closed with a super-glue called Dermabond. The researchers at the University of Massachusetts believe Dermabond may be a safe alternative to using staples at the time of a cesarean delivery, but this has not been studied. Women who choose to participate will be randomly assigned to have the cesarean delivery skin incision closed with staples or Dermabond. The researchers will survey the patients to see how they felt about the experience and the appearance of their scar. The researchers will survey physicians performing the surgery to see how easy Dermabond was to use. The researchers will ask physicians to evaluate the appearance of the incision after a 6-week recovery period and will analyze complications (such as bruising, infection, or separation of the wound) in the two groups.

Conditions

Interventions

TypeNameDescription
DEVICESurgical skin staplesStandard method to close abdominal surgical wounds
DEVICEDermabondAlternative method (superglue) to close abdominal surgical wounds

Timeline

Start date
2007-09-01
Primary completion
2012-05-01
Completion
2012-05-01
First posted
2007-09-03
Last updated
2013-03-05
Results posted
2013-03-05

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00524511. Inclusion in this directory is not an endorsement.