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Comparing the Effect of Intravenous Aminophylline and Ondansetron on Incidence of Post-Dural Puncture Headache in Cesarean Section Surgeries

Phase 2
Conditions
caesarean section.
Delivery by elective caesarean sectio
Registration Number
IRCT2016110519470N50
Lead Sponsor
Vice Chancellor for Research, Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
300
Inclusion Criteria

women undergoing elective cesarean section under spinal anesthesia ASA class II- I.

Exclusion criteria: pregnant women; heart disease; chronic liver and kidney failure; migraine headaches and stress; chronic hypertension; gestational hypertension; pre-eclampsia; seizures; psychiatric problems; allergy to ondansetron; aminophylline and theophylline; history of drug addiction; failed to spinal anesthesia or more than once spinal anesthesia attempts.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Headache. Timepoint: every 72, 48, 24 hours in 3 days after surgery. Method of measurement: Numerical rating scale (NRS).;Nausea and vomiting. Timepoint: every 72, 48, 24 hours in 3 days after surgery. Method of measurement: Observasion.
Secondary Outcome Measures
NameTimeMethod
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