Effect of oral lorazepam on headache caused by spinal anesthesia in cesarean sectio
Phase 3
Not yet recruiting
- Conditions
- Single liveborn infant, delivered by cesareanSpinal anesthesia in cesarean section.Z38.01
- Registration Number
- IRCT20210921052542N1
- Lead Sponsor
- Kermanshah University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 178
Inclusion Criteria
Women undergoing cesarean section by spinal anesthesia
From 15 years old to 45 years old
Perfect vision
Having the consent to participate in the study
ASA=1,2
Exclusion Criteria
Patients with allergies to benzodiazepines
History of migraine headaches
mental health problems
Reluctance to continue collaborating in the study
Perform re-spinal anesthesia
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Headache. Timepoint: Times before and after the intervention and up to 7 days after cesarean section. Method of measurement: Visual analogue scale ( VAS ) Questionnaire.
- Secondary Outcome Measures
Name Time Method