Trials / Terminated
TerminatedNCT01169064
Topical Silver for Prevention of Wound Infection After Cesarean Delivery
Topical Silver for Prevention of Wound Infection Post Cesarean Delivery: A Randomized Controlled Trial
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 475 (actual)
- Sponsor
- Vanderbilt University · Academic / Other
- Sex
- Female
- Age
- 18 Years – 50 Years
- Healthy volunteers
- Not accepted
Summary
A common concern in any surgical procedure is the occurrence of infection. Silver-containing treatments are popular and used in wound treatment; however, there is presently little evidence of the effectiveness of silver-containing treatment for the prevention of obstetrical wound infection. We plan to investigate the rate of infection in women experiencing cesarean sections at Vanderbilt University Medical Center (VUMC) by comparing the infection rate based on a randomized choice of silver-containing wound dressings to soft cloth adhesive wound dressings.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Silver-containing surgical dressing | Dressing placed over surgical incision and remain for 3-5 days |
| DEVICE | Cloth adhesive dressing | Cloth adhesive dressing placed over surgical incision and remains for 3-5 days |
Timeline
- Start date
- 2010-07-01
- Primary completion
- 2012-07-01
- Completion
- 2012-07-01
- First posted
- 2010-07-23
- Last updated
- 2017-05-30
- Results posted
- 2017-05-30
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01169064. Inclusion in this directory is not an endorsement.