Trials / Completed
CompletedNCT03120806
Interrupted Versus Continuous Subcuticular Skin Suturing in Elective Cesarean Section.
Comparative Study Between Interrupted and Continuous Subcuticular Skin Suturing in Women Undergoing Elective Cesarean Section. A Randomized Controlled Trial
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 169 (actual)
- Sponsor
- Cairo University · Academic / Other
- Sex
- Female
- Age
- 19 Years – 39 Years
- Healthy volunteers
- Not accepted
Summary
Non-diabetic pregnant women who undergo elective CS will be randomized into two groups: group I included women who has their skin closed with subcuticular interrupted mattress suture using non-absorbable polypropylene, and group II included women who has their skin closed with subcuticular continous suture using the same suture material
Detailed description
Non-diabetic pregnant women who undergo elective CS will be randomized into two groups: group I included women who had their skin closed with subcuticular interrupted mattress suture using non-absorbable polypropylene, and group II included women who had their skin closed with subcuticular continous suture using the same suture material.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Interrupted subcuticular skin closure | skin is closed with interrupted mattress subcuticular sutures using non-absorbable polypropylene after elective cesarean section |
| PROCEDURE | continuous subcuticular skin closure | skin is closed with continuous subcuticular sutures using non-absorbable polypropylene after elective cesarean section |
Timeline
- Start date
- 2017-04-16
- Primary completion
- 2017-12-01
- Completion
- 2017-12-20
- First posted
- 2017-04-19
- Last updated
- 2021-12-23
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT03120806. Inclusion in this directory is not an endorsement.