Degenerative joint disease.
Conditions
Interventions
Intervention 1: Control group: Epidural block group In this trial, our treatment method was performed to reduce pain after knee replacement surgery.10 to 15 cc bupivacaine is 0.25%, which is injected
Sponsors
Iran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
40 Years to 70 Years
Inclusion criteria
Inclusion criteria: age between 40-70 years ASA I , II having the satisfaction of participating in the study
Exclusion criteria
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSara zamani
Iran University of Medical Sciences
Outcome results
None listed