comparison of headache accurance and severity after use of phenylephtine and ephedrine for treatment of hypotention during cesarian delivery under spinal anesthesia
Phase 2
- Conditions
- headache.Drug-induced headache, not elsewhere classified
- Registration Number
- IRCT201509042946N7
- Lead Sponsor
- Vice chancellor for reasearch ,Kermanshah University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 105
Inclusion Criteria
Pregnant women aged 18 to 40 years; ASA class I_II; systolic blood pressure 120-140 mmhg; body mass index 18.5_25 and normal single fetus pregnancy.
Exclusion criteria: History of migraine; psychiatric disorders; any medication except pregnancy supplements; presence of headache in admission time to operation room; eclampsia; preeclampsia; hypertention; diabetes mellitus and cardiovascular disease.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Headache incidence and intencity. Timepoint: during cesarean, 1, 6, 24 hours later. Method of measurement: by visual analogue scale.
- Secondary Outcome Measures
Name Time Method Vital sign changes. Timepoint: every 2 minute until 10minute then every 5 minute. Method of measurement: by datascope monitor.