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Comparison of Outcome Between (ERACS) Versus Traditional Methods in Elective CS — ERACS  

ERAS Clinical Trial

Official title:
Comparison of Outcome Between the Implementation of Enhanced Recovery After Elective Cesarean Section Protocol (ERACS) Versus Traditional Methods

Clinical Trial Summary

The study is designed to evaluate the effect of implementing enhanced recovery after surgery (ERAS) protocol during elective cesarean section on patient's outcome measures.

Clinical Trial Description

The study is designed to evaluate the effect of implementing enhanced recovery after surgery (ERAS) protocol during elective cesarean section on patient outcome measures. The primary outcome is the evaluation of inpatient postpartum recovery using the Obstetric Quality of Recovery 11 score (ObsQoR-11) at the time of discharge. Secondary outcomes are the evaluation of peak numeric postoperative pain rating score within the postoperative hospital stay, total amount of postoperative opioid consumption, postoperative nausea, and vomiting impact score after 6 hours postoperatively and at time of discharge, patient satisfaction using Leiden perioperative care patient satisfaction questionnaire (LPPSq) at time of discharge, presence of post-cesarean ileus and Hospital length to achieve criteria for discharge. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06225557
Study type Interventional
Source Minia University
Contact Marwa AA Mohamed, AS Lecturer
Phone 00201005431155
Email marwaelhelaly@hotmail.com
Status Not yet recruiting
Phase N/A
Start date March 10, 2024
Completion date June 30, 2024
View Details
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