Clinical Trials Directory

Trials / Completed

CompletedNCT01211600

Cesarean Trial of Staples vs. Sutures

Cesarean Randomized Control Trial Of Sutures vs. Staples (CROSS)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
746 (actual)
Sponsor
Thomas Jefferson University · Academic / Other
Sex
Female
Age
Healthy volunteers
Accepted

Summary

To determine whether the rate of wound complications differs based on method of closure of skin incision (staples vs. suture) after cesarean delivery.

Detailed description

Despite this large number of cesareans performed annually, there is a paucity of data to suggest which technique is superior for closure of the skin incision with regards to wound complications, including wound separation and infection. As the morbidity associated with a cesarean delivery is usually related to wound complications, especially infection, we feel that it is important to examine this outcome by comparing the current skin closure techniques: staples versus suture.

Conditions

Interventions

TypeNameDescription
OTHERStaplesInterrupted Ethicon Staples
OTHERSutureSubcuticular continuous suture (4-0 Monocryl Plus on PS2 needle or 4-0 Vicryl Plus on FS2 or PS2 needle)

Timeline

Start date
2010-06-01
Primary completion
2014-10-01
Completion
2014-12-01
First posted
2010-09-29
Last updated
2019-11-26
Results posted
2019-11-26

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01211600. Inclusion in this directory is not an endorsement.