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Effect of Visceral and Parietal Peritoneum Suturation on Postoperative Vital Signs

Effect of Visceral and Parietal Peritoneum Suturation on Postoperative Vital Signs

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02581293
Enrollment
132
Registered
2015-10-20
Start date
2015-03-31
Completion date
2016-02-29
Last updated
2015-10-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Pain

Brief 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.

Interventions

PROCEDUREGroup 1: Only visceral peritoneum will be closed
PROCEDUREGroup 2 : Only parietal peritoneum will be closed
PROCEDUREGroup 3 : Both of them will be closed
PROCEDUREGroup 4: None of them will be closed

Sponsors

Zeynep Kamil Maternity and Pediatric Research and Training Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SCREENING
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
No minimum to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Women underwent uncomplicated c-section

Exclusion criteria

* Patient with systemic Diseases * Pregnant with Obstetric complications * Pregnant with two or more previous c-sections

Design outcomes

Primary

MeasureTime frame
Postoperative vital sign (arterial tension)First postoperative hour

Countries

Turkey (Türkiye)

Contacts

Primary ContactMeryem Kurek EKEN, MD
meryemkurek@yahoo.com+905305104468

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026