Clinical Trials Directory

Trials / Completed

CompletedNCT04364607

IM Neostigmine for Accelerating Bladder Emptying After CS by Spinal Anesthesia

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

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
100 (actual)
Sponsor
Mansoura University · Academic / Other
Sex
Female
Age
20 Years – 35 Years
Healthy volunteers
Not accepted

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

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGNeostigmineParticipants will receive 0.5 mg IM neostigmine
DRUGNaCl 0.9%Participants will receive IM NaCl 0.9% as a placebo

Timeline

Start date
2020-08-05
Primary completion
2021-10-26
Completion
2021-10-26
First posted
2020-04-28
Last updated
2023-06-07

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04364607. Inclusion in this directory is not an endorsement.