Clinical Trials Directory

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

TypeNameDescription
DEVICESilver-containing surgical dressingDressing placed over surgical incision and remain for 3-5 days
DEVICECloth adhesive dressingCloth 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.