Evaluation of Intranasal oxytocine spray effect on preventing post-dural puncture headache after cesarean sectio

Phase 3

• Conditions: post-dural puncture headache.; Spinal and epidural anesthesia-induced headache during the puerperium; O89.4

• Registration Number: IRCT20201215049725N1
• Lead Sponsor: Karaj University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 29 August 2022

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 170

Inclusion Criteria

Elective cesarean candidates

Exclusion Criteria

Allergies to drugs used in this study
BMI more than 35
Hepatic, renal or cardiac disorder
Neuromuscular disease
History of lumbar discopathy / history of neuropathy
Opioids or analgesic usage 3 days before the study
Consumption of calcium channel blockers

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Headache severity after spinal anesthesia based on vas-score. Timepoint: 12, 24, 48, 72 hours after cesarean section. Method of measurement: Visual Analogue Scale.