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Effect of low dose intravenous ketamine versus placebo on the prevention of headache after spinal anesthesia in patients who are candidates for cesarean sectio

Phase 3
Recruiting
Conditions
Headache.
Tension-type headache, unspecified
G44.20
Registration Number
IRCT20120215009014N387
Lead Sponsor
Hamedan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
70
Inclusion Criteria

Age: 16 to 45 years old
Candidates for elective cesarean section

Exclusion Criteria

History of heart, respiratory, renal, or neurologic diseases
History of chronic headache or migraine
History of allergy to anesthesia medications
Preeclampsia

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Headache. Timepoint: On the first to the third days after surgery. Method of measurement: Using Visual Analog Scale (VAS).
Secondary Outcome Measures
NameTimeMethod
Vomiting. Timepoint: During surgery. Method of measurement: By clinical observation.
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