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
| Type | Name | Description |
|---|---|---|
| DEVICE | Surgical skin staples | Standard method to close abdominal surgical wounds |
| DEVICE | Dermabond | Alternative 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.