Trials / Unknown
UnknownNCT02581293
Effect of Visceral and Parietal Peritoneum Suturation on Postoperative Vital Signs
- Status
- Unknown
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 132 (estimated)
- Sponsor
- Zeynep Kamil Maternity and Pediatric Research and Training Hospital · Academic / Other
- Sex
- Female
- Age
- 40 Years
- Healthy volunteers
- Accepted
Summary
In this study the investigators want to asses the effect of peritonisation at c-section on postoperative vital signs which was thought to be an indirect finding secondary to increased sympathetic activity originated from pain caused by stretched peritoneum.
Detailed description
At c-section subject will be randomised into four groups: Group1: Only visceral peritoneum will be closed Group 2: Only parietal peritoneum will be closed Group 3: Both of them will be closed Group 4: None of them will be closed During the postoperative period all patients will undergo vital sign screening including urine output, blood pressure measurement, pulse rate and VAS score will be determined at post operative 6th hour and 24th hour.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Group 1: Only visceral peritoneum will be closed | |
| PROCEDURE | Group 2 : Only parietal peritoneum will be closed | |
| PROCEDURE | Group 3 : Both of them will be closed | |
| PROCEDURE | Group 4: None of them will be closed |
Timeline
- Start date
- 2015-03-01
- Primary completion
- 2015-10-01
- Completion
- 2016-02-01
- First posted
- 2015-10-20
- Last updated
- 2015-10-20
Locations
1 site across 1 country: Turkey (Türkiye)
Source: ClinicalTrials.gov record NCT02581293. Inclusion in this directory is not an endorsement.