None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: INCLUSION CRITERIA 1. Male or female 2. Age >40 or <80 3. ASA physical status I and II 4. All ethnic or racial groups 5. Suffering from osteoarthritis and scheduled for primary unilateral total knee arthroplasty
Exclusion criteria
Exclusion criteria: 1. Age <40 yr or >80 yr. 2. ASA physical status more than II. 3. Refusal of patient for participation. 4. Allergy to local anesthetics. 5. History of opioid dependence. 6. Contraindications to spinal anaesthesia, femoral nerve block, or sciatic nerve block (coagulation defects, infection at puncture site, pre-existing neurological deficits in the lower extremities); inability to use patient-controlled analgesia (IV PCA). 7. Contraindications for NSAID (NSAID or aspirin allergy, severe liver disease, or serum creatinine 2.0 mg/dL), weight >140 kg, and recent steroid use (<53 months). Complaints of painful polyarthalgia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| ? To compare continuous femoral nerve blockade and continuous epidural analgesia in terms of post operative pain relief in patients undergoing knee arthroplasty. ? To compare patient?s ease during postoperative physiotherapy associated with the two techniques Timepoint: First two days for pain and ease of physiotherapy | — |
Secondary
| Measure | Time frame |
|---|---|
| ? To compare the side effects associated with the two techniques. ? Patient?s overall satisfaction from surgery and anesthesia at the end of three and six months. Timepoint: The side effects for first two days and patient's overall satisfaction for next six months | — |
Countries
India