Hemodynamic Changes of Spinal Anesthesia in Pre-eclampsia
Phase 1
- Conditions
- Pre-eclampsia.Moderate Pre-eclampsia
- Registration Number
- IRCT201304157695N3
- Lead Sponsor
- Vice-Chancellor for Research of Qazvin University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 70
Inclusion Criteria
Pregnant women with age range of 18-45 years old
Exclusion criteria:
Patient refusal of spinal anesthesia, presence of: fetal distress, convulsion, pulmonary edema, headache, visual impairment, impaired consciousness, coagulopathy, high systemic blood pressure (BP>170/110), systemic involvement (diabetes mellitus, chronic hypertension), positive history of antihypertensive drugs consumption
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Blood pressure and heart rate. Timepoint: After spinal anesthesia, every 5 minutes during operation until 30 minutes after operation in recovery period. Method of measurement: By noninvasive cardiovascular monitoring, blood pressure and heart rate were measured and recorded in questionnaire.
- Secondary Outcome Measures
Name Time Method Shivering. Timepoint: Recovery period. Method of measurement: By observational method (mild, moderate and sever) was determined and recorded in questionnaire.;Nausea, vomiting. Timepoint: During operation until 30 minutes after operation in recovery period. Method of measurement: By observational method (mild, moderate and sever) was determined and recorded in questionnaire.;Postoperative Pain. Timepoint: During 30 minutes after operation in recovery period. Method of measurement: By Visual Analog Scale was determined and recorded in questionnaire.;Apgar score. Timepoint: First and fifth minute. Method of measurement: By numbering method (1-10) was determined and recorded in questionnaire.