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Continuous intra-articular levobupivicaine after unicondylar knee replacement - a randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN62841244
Enrollment
Unknown
Registered
2006-09-29
Start date
2005-08-01
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

Musculoskeletal Diseases: Unicondylar Knee Replacement (UKR) Musculoskeletal Diseases Unicondylar Knee Replacement (UKR)

Interventions

1. One group receiving a postoperative intra-articular infusion of local anaesthetic 2. Control group receiving a saline infusion

Sponsors

Record Provided by the NHSTCT Register - 2006 Update - Department of Health (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Not provided at time of registration

Exclusion criteria

Exclusion criteria: Not provided at time of registration

Design outcomes

Primary

MeasureTime frame
Pain - Visual Analogue score, use of additional analgesia postop (e.g. PCA, Oramorph).—

Secondary

MeasureTime frame
Not provided at time of registration—

Countries

United Kingdom

Outcome results

None listed

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