effect of continuous epidural and continuous paravertebral block on pain after knee arthroplasty surgery
Phase 3
- Conditions
- Degenerative joint disease.
- Registration Number
- IRCT20191013045095N1
- Lead Sponsor
- Iran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 39
Inclusion Criteria
age between 40-70 years
ASA I , II
having the satisfaction of participating in the study
Exclusion Criteria
sensitivity to any of the drugs used in the study
Body mass index>40
severe liver and heart disease
addiction or prolonged use of analgesics
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain following joint changes leading to surgery and knee replacement. Timepoint: Immediately after the intervention 4 hours after the intervention 8 hours after the intervention 16 hours after the intervention 24 hours after the intervention. Method of measurement: Pain intensity with VAS scale numbered by a ruler on a scale of 0 to 10.
- Secondary Outcome Measures
Name Time Method Age. Timepoint: 0. Method of measurement: Year.;Sex. Timepoint: 0. Method of measurement: Male or female.;Weight. Timepoint: 0. Method of measurement: Different number by kilogram.;Side effects of anesthesia. Timepoint: 24 hours. Method of measurement: Patient symptoms.;Side effects of mepridine. Timepoint: 24 hours. Method of measurement: Patient symptoms.;Amount of mepridine. Timepoint: 24 hours. Method of measurement: By used dosage.