Clinical Trials Directory

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

TypeNameDescription
DRUGintravenous 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.
DRUGNeostigmine 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.