Trials / Not Yet Recruiting
Not Yet RecruitingNCT06493838
Clinical Efficacy of Prophylactic Intravenous Neostigmine and Atropine in Preventing Post-Dural Puncture Headache Among Parturient Undergoing Spinal Anesthesia for Cesarean Section: A Double-blind Randomized Placebo-controlled Trial
- Status
- Not Yet Recruiting
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 180 (estimated)
- Sponsor
- Minia University · Academic / Other
- Sex
- Female
- Age
- 18 Years – 35 Years
- Healthy volunteers
- Not accepted
Summary
Post dural puncture headache is a distressing issue, many measures tried to treat symptoms but few delt with prevention.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | intravenous 50 mL of saline injection of 0.9% after umbilical cord clamping. | intravenous 50 mL of saline injection of 0.9% after umbilical cord clamping. |
| DRUG | Neostigmine 20μg/kg (Neostigmine Methylsulphate 0.5 mg, Amriya Pharm.Ind.) and atropine 0.01 mg/kg (diluted in 50 ml saline; 0.9% for 10 min) following umbilical cord clamping. | Neostigmine 20μg/kg (Neostigmine Methylsulphate 0.5 mg, Amriya Pharm.Ind.) and atropine 0.01 mg/kg (diluted in 50 ml saline; 0.9% for 10 min) following umbilical cord clamping. |
Timeline
- Start date
- 2024-07-15
- Primary completion
- 2025-01-15
- Completion
- 2025-01-16
- First posted
- 2024-07-10
- Last updated
- 2024-07-16
Source: ClinicalTrials.gov record NCT06493838. Inclusion in this directory is not an endorsement.