Comparison of Phenylephrine and Ephedrine in the treatment of hypotensio
Not Applicable
- Conditions
- Hypotension.Hypotension due to drugs
- Registration Number
- IRCT2015070920588N3
- Lead Sponsor
- Vce chancellor for research of Isfahan University of Medical Scienses
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 110
Inclusion Criteria
inclusion criteria: 110 patient with ASA physical status class I-II aged 40-65 years who are candidates of lower extremity orthopedic surgery.
Exclusion criteria:Any hypersensitivity reaction to vasopressore or local anesthetic drugs, systemic diseases like cardiovascular, liver, or renal diseases and pregnancy.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Systolic blood pressure. Timepoint: 2, 4, 6, 8, 10, 14, 20 and 30 minutes after arrival of the patient to the recovery room. Method of measurement: Noninvasive Blood pressure monitoring system.;Diastolic blood pressure. Timepoint: 2, 4, 6, 8, 10, 14, 20 and 30 minutes after arrival of the patient to the recovery room. Method of measurement: Noninvasive Blood pressure monitoring system.;Mean arterial blood pressure. Timepoint: 2, 4, 6, 8, 10, 14, 20 and 30 minutes after arrival of the patient to the recovery room. Method of measurement: Noninvasive Blood pressure monitoring system.
- Secondary Outcome Measures
Name Time Method Heart rate. Timepoint: 2 ?4 ? 6 ? 8 ? 10 ? 14 ? 20 and 30 minutes after arrival of the patient to the recovery room. Method of measurement: pulse oxymetery.;Arterial blood oxygen saturation. Timepoint: 2 ?4 ? 6 ? 8 ? 10 ? 14 ? 20 and 30 minutes after arrival of the patient to the recovery room. Method of measurement: pulse oxymetery.;Drug and non drug related complications. Timepoint: Any time during the study. Method of measurement: clinical evaluation.