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
| Type | Name | Description |
|---|---|---|
| OTHER | Staples | Interrupted Ethicon Staples |
| OTHER | Suture | Subcuticular 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.