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NCT03326180: SPAARK

Study of Peri-Articular Anaesthetic for Replacement of the Knee

Completed Phase 3 Last updated 4 November 2022
What this trial tests

Phase 3 trial testing Liposomal bupivacaine in Knee Osteoarthritis in 533 participants. Completed in 21 April 2021.

Timeline
29 March 2018
Primary endpoint
28 February 2021
21 April 2021

Quick facts

Lead sponsorUniversity of Leeds
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment533
Start date29 March 2018
Primary completion28 February 2021
Estimated completion21 April 2021
Sites11 locations across United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

University of Leeds

Who can join

18 and older, any sex, with Knee Osteoarthritis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The clinical and cost effectiveness of peri-articular liposomal bupivacaine plus bupivacaine hydrochloride compared with bupivacaine hydrochloride alone for post-operative recovery after knee replacement surgery: A multi-centre, patient-blinded, randomised controlled trial.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Liposomal bupivacaine

Trials testing the same drug.

Other recruiting trials for Knee Osteoarthritis

Currently open trials in the same condition.

Other University of Leeds 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/NCT03326180.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing