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
| Type | Name | Description |
|---|---|---|
| DRUG | Neostigmine | Participants will receive 0.5 mg IM neostigmine |
| DRUG | NaCl 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.