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Peritoneal Irrigation at Elective Cesarean Section

Comparative Study Between Intraabdominal Irrigation and Non Irrigation During Elective Cesarean Section

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03413748
Enrollment
200
Registered
2018-01-29
Start date
2018-01-31
Completion date
2018-07-31
Last updated
2018-01-29

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

Conditions

Postoperative Recovery

Brief summary

All participants will be randomized at elective cesarean section to either irrigation with 500 to 1000 ml of warm normal saline after closure of visceral peritoneum or non irrigation

Detailed description

All participants will be randomized at elective cesarean section to either irrigation with 500 to 1000 ml of warm normal saline after closure of visceral peritoneum or non irrigation during the procedure of elective lower segment cesarean section

Interventions

PROCEDUREElective Cesarean Section

lower segment cesarean section

Irrigation of peritoneal cavity with 500 - 1000 ml of warm normal saline

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Singleton pregnancy * Gestational age 36 - 40 weeks * Elective Cesarean section * Under spinal anaesthesia

Exclusion criteria

* Chronic diseases as Diabetes and hypertension * Intestinal diseases as Crohn's disease * Psychological and neurological conditions affecting pain sensation * women with ferbrile morbidity before the operation * The need for general anesthesia

Design outcomes

Primary

MeasureTime frameDescription
Intestinal recovery24 hours after operationAuscultation of intestinal sounds

Secondary

MeasureTime frameDescription
Temperatureevery hour for 16 hours after the operationmeasuring the oral temperature by thermometer
postoperative pain24 hours after surgeryPain score felt by the patient using Visual analogue score

Countries

Egypt

Contacts

Primary ContactAhmed Maged, MD
prof.ahmedmaged@gmail.com+2001005227404
Backup ContactAmira Yehia, MD
amira_el_sayed_yehia@hotmail.com

Outcome results

None listed

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