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NCT04382144: LELIBU

Levobupivacaine Versus Liposomal Bupivacaine (Exparel®) for Treatment of Pain and Disability in Lateral Epicondylitis

Status unknown Phase 4 Last updated 11 May 2020
What this trial tests

Phase 4 trial testing Liposomal bupivacaine in Tennis Elbow in 50 participants. Status unknown.

Timeline
1 September 2020
Primary endpoint
31 December 2021
1 May 2022

Quick facts

Lead sponsorTurku University Hospital
PhasePhase 4
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingsingle
Primary purposetreatment
Enrollment50
Start date1 September 2020
Primary completion31 December 2021
Estimated completion1 May 2022

Drugs / interventions tested

Conditions studied

Sponsor

Turku University Hospital

Who can join

Adults 18 to 65, any sex, with Tennis Elbow or Lateral Epicondylitis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The main objective of the trial is to compare the effectiveness of injected levobupivacaine and liposomal bupivacaine in the treatment of pain and disability in patients with lateral epicondylitis. Primary outcome is pain (VAS) at 1 week and at 1 month after injection. Secondary outcomes are the Quick Disabilities of the Arm, Shoulder and Hand DASH (Quick DASH) and Oxford Elbow Score (OES) and a record of time off work due to lateral epicondylitis in days at 1 week and at 1 month. The study will be a cross-over trial

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Liposomal bupivacaine

Trials testing the same drug.

Other recruiting trials for Tennis Elbow

Currently open trials in the same condition.

Other Turku University Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04382144.

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