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Comparison of Extraperitoneal and Intraperitoneal Cesarean Technique

Comparison of Extraperitoneal and Intraperitoneal Cesarean Technique: Double Blind Controlled Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02760290
Enrollment
50
Registered
2016-05-03
Start date
2016-03-31
Completion date
2016-07-31
Last updated
2022-03-15

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

Conditions

Hemorrhage, Ileus, Pain, Postpartum Fever

Keywords

Forced Expiratory Volume in 1 second, Forced expiratory vital capacity, Peak expiratory flow

Brief summary

Cesarean section will performed via intraperitoneally and extraperitoneally. During postoperative period pain, need for analgesia, respiratory function tests, ileus, bowel movement, discharged time will be compared.

Detailed description

Investigators will compared results intra and extraperitoneal cesarean section. Two groups will determine according to random numbers table. After operations, blood count, C reactive proteins, postoperative temperature, need for analgesia, ileus, bowel movement, mobilization time will compare by blind physician. Abdominal, shoulder and incisional pain at postoperative 0, 6, 12, 18, 24, 30 hours will compared by use visual analog score. Neonatal results and complications also will compare. Investigators and participants will be blind regarding technique.

Interventions

PROCEDUREExtraperitoneal cesarean section
PROCEDUREIntraperitoneal cesarean section

Sponsors

Zeynep Kamil Maternity and Pediatric Research and Training Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Cesarean section for any reasons

Exclusion criteria

* Involuntary

Design outcomes

Primary

MeasureTime frame
Pain Scores as measured by the Visual Analog Scale2 days

Secondary

MeasureTime frame
C reactive proteins level2 days
Complications2 days
Discharge time4 days
Blood count2 days
Forced vital capacity2 days
Peak expiratory flow2 days
Forced expiratory volume in 1 second2 days

Countries

Turkey (Türkiye)

Outcome results

None listed

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