Peritoneal Irrigation at Elective Cesarean Section

Postoperative Recovery Clinical Trial

Official title:

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

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03413748
• Other study ID #: 23
• Status: Not yet recruiting
• Phase: N/A
• First received: January 22, 2018
• Last updated: January 26, 2018
• Start date: January 2018
• Est. completion date: July 2018

Study information

• Verified date: January 2018
• Source: Cairo University
• Contact: Ahmed Maged, MD
• Phone: +2001005227404
• Email: prof.ahmedmaged[@]gmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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

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

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 200
• Est. completion date: July 2018
• Est. primary completion date: June 2018
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 20 Years to 40 Years

Eligibility

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

Related Conditions & MeSH terms

• Postoperative Recovery

Intervention

Procedure:
• Elective Cesarean Section
lower segment cesarean section

Other:
• Peritoneal irrigation
Irrigation of peritoneal cavity with 500 - 1000 ml of warm normal saline

Locations

Country	Name	City	State
Egypt	Kasr Alainy medical school	Cairo

Sponsors (1)

Lead Sponsor	Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Intestinal recovery	Auscultation of intestinal sounds	24 hours after operation
Secondary	Temperature	measuring the oral temperature by thermometer	every hour for 16 hours after the operation
Secondary	postoperative pain	Pain score felt by the patient using Visual analogue score	24 hours after surgery