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IM Neostigmine for Accelerating Bladder Emptying After CS by Spinal Anesthesia

Cesarean Section Complications Clinical Trial

Official title:
Intramuscular Neostigmine for Accelerating Bladder Emptying After Cesarean Section by Spinal Anesthesia

Clinical Trial Summary

The aim of this study is to assess the efficacy of IM neostigmine (0.5 mg) for acceleration of bladder evacuation and prevention of postoperative urine retention following cesarean delivery carried out under spinal anesthesia

Clinical Trial Description

Following cesarean delivery, women will receive either 0.5 mg IM neostigmine (study group) or IM NaCl 0.9% (control group). Bladder ultrasonography will be done every hour until spontaneous voiding occurs. If postoperative urine retention occurred (void inability with bladder volume > 600 ml by ultrasound), urinary catheterization will be done. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04364607
Study type Interventional
Source Mansoura University
Contact
Status Completed
Phase Phase 4
Start date August 5, 2020
Completion date October 26, 2021
View Details
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