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Enhanced Recovery After Cesarean Section With Low Dose Intrathecal Morphine.

Pain, Postoperative Clinical Trial

Official title:
Enhanced Recovery After Cesarean Section With Low Dose Intrathecal Morphine. A Prospective Randomized Controlled Study.

Clinical Trial Summary

This study is designed to see the effect of low dose intrathecal morphine on promting enhanced recovery after cesarean delivery with early ambulation and reduction of hospital stay.

Clinical Trial Description

Parturients showing for elective cesarean section will be randomized into 3 groups by a computer generated randomization list. Each randomization slip will be put in a sealed envelope until patient enrollment. Patients will be divided into Group C: control group, given intrathecal bupivacaine 12.5 mg. Group M25: intrathecal bupivacaine 12.5mg + morphine 25 microgram. Group M50: intrathecal bupivacaine 12.5mg + morphine 50 microgram. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04618146
Study type Interventional
Source Minia University
Contact Sohair A Megalla, MD
Phone +20 120 003 6447
Email Sohair.Adeeb@minia.edu.eg
Status Recruiting
Phase N/A
Start date November 10, 2020
Completion date March 2021
View Details
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