Unilateral knee arthroplasty. Unspecified complication of internal orthopedic prosthetic device, implant and graft, initial encounter
Conditions
Interventions
Intervention 1: Intervention group: The intervention group will receive 0.25% bupivacaine to adductor canal block after unilateral knee arthroplasty. Intervention 2: Control group: The control group w
Sponsors
Mashhad University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Months to No maximum
Inclusion criteria
Inclusion criteria: Patients with ASA I or II, who are candidate for unilateral knee arthroplasty Age over 18 years BMI less than 35
Exclusion criteria
Exclusion criteria: History of neuropathy Having coagulation disorder Drug abuse Having local anesthetics allergies
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The rate of pain. Timepoint: 3, 6, 12 and 24 hours after intervention. Method of measurement: Visual analogue scale (VAS).;Muscle strength. Timepoint: 12 and 24 hours after intervention. Method of measurement: Maximum voluntary isometric contraction (MVIC). | — |
Secondary
| Measure | Time frame |
|---|---|
| The rate of pain reliever consumption. Timepoint: 24 hours after intervention. Method of measurement: Type and amount of pain reliever consumed by the patient. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactHosnieh Esmaeili Namghi
Mashhad University of Medical Sciences
Outcome results
None listed