Effect of voluven on post spinal headache in patients with cesarean sectio
Phase 2
- Conditions
- Post spinal headache.Other specified headache syndromes
- Registration Number
- IRCT201308243305N5
- Lead Sponsor
- Vice-chancellor Of Research Babol University Of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 200
Inclusion Criteria
Inclusion Criteria: All of patients who are candidates for Cesarean section with Spinal anesthesia.
Exclusion Criteria
Patients contraindicated of LP; psychotic or patients with space occupying lesion; addicts; corticosteroid and NSAID users.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Headache. Timepoint: daily until one week post spinal headache. Method of measurement: Question & answer.
- Secondary Outcome Measures
Name Time Method Blood pressure. Timepoint: During spinal anesthesia. Method of measurement: BP Cuff.;Heart rate. Timepoint: During spinal anesthesia. Method of measurement: ECG.;Nausea & Vomiting. Timepoint: During spinal anesthesia. Method of measurement: Question & answer.;Arterial oxygen saturation. Timepoint: During spinal anesthesia. Method of measurement: pulse oximeter.