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Perioperative Analgesia for Knee Arthroplasty (PAKA) - a pilot randomised trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN29107680
Enrollment
46
Registered
2011-06-01
Start date
2010-01-01
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Muskuloskeletal, total knee arthroplasty, analgesia Musculoskeletal Diseases Knee Arthroplasty

Interventions

Femoral nerve block using 30ml of Levobupivicaine 0.25% versus Peri-articular infiltration of multimodal agents consisting of 150mg of Levobupivacaine, 10mg Morphine and 30mg Ketorolac diluted in 0.9%

Sponsors

University of Warwick (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients undergoing an elective primary unilateral total knee replacement (TKA) under the care of an orthopaedic consultant at University Hospitals Coventry and Warwickshire NHS Trust

Exclusion criteria

Exclusion criteria: 1. Cognitive impairment, unable to complete questionnaire 2. Patients who lack capacity under the Mental Capacity Act 2005 3. Patients with pre-operative history of neruological abnormality in the ipsilateral leg e.g. history of stroke, neurogenic pain or previous nerve injury 4. Patients having spinal aneasthesia 5. Patients with specific contraindication to the analgesic agents used: Morphine, Ketorolac, Levobupivicaine

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale at 18 hours post operation

Secondary

MeasureTime frame
Serum Levobupivacaine levels pre & post retransfusion 1. Functional assessment: 1.1. Straight leg raise 1.2. Mobility assessed bed to chair 18 & 48 hours post operatively 2. Oxford Knee Score 6 weeks post operatively

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026