The comparison between effect of orally propranolol lorazpam and propranolol-lorazpam in reduction of preoperative anexiety
Phase 2
- Conditions
- eurotic, stress-related and somatoform disorders.Phobic anxiety disorder, unspecified
- Registration Number
- IRCT201106146256N2
- Lead Sponsor
- vice-chancellor for research of Qazvin universityof medical science
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 75
Inclusion Criteria
Grasp testimonial; elective minor to moderate surgery as: inguinal hernia, trans urethral lithothomy , colles fx, tibia fx; age 18-45 and ASA class Iand II
Exclusion criteria:
History of chronic consumption of bzd antipsychotics, opium and amphetamines; history of panic attack or any psychologic disorder; history of CHF, asthma COPD ,dm type Iand II; history of hypertension; history of any anti hypertension drug consumption and history of any food and drugs allergy
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Preoprative stress score. Timepoint: 10 hours. Method of measurement: APIAS SCALE.
- Secondary Outcome Measures
Name Time Method Blood pressure. Timepoint: 15 mint. Method of measurement: Non-Invasive Blood Pressure (NIBP).;Heart rate. Timepoint: 15min. Method of measurement: beat/min.