Effect of Neostigmine and Atropine on post dural puncture headache in spinal anesthesia in cesarea

Phase 3

Recruiting

• Conditions: Cesarean section.; Delivery by caesarean section, unspecified; O82.9

• Registration Number: IRCT20210324050762N1
• Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 1 November 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 62

Inclusion Criteria

Pregnant woman candidate for cesarean section with spinal anesthesia
American anesthesiologists association classification I and II
Age 18-45 years
No neurological deficit in limb, spinal cord and CNS
No coagulation diseases
No history of spinal cord surgery, spinal canal stenosis and MS
Duration of surgery less than 2 hours
No heart conductive disorder
No history of migraine headaches
No anticoagulant drug consumption
Consent for spinal block
Patient consent to participate in the study

Exclusion Criteria

Spinal block failure
Change in anesthesia method to general anesthesia
Bleeding more than 20 cc/kg
More than 3 punctures

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Headache severity. Timepoint: From first day to five days after surgery. Method of measurement: Visual Analogue Scale (VAS).;Duration of headache. Timepoint: From first day to five days after surgery. Method of measurement: Counting the number of days suffering from headache.