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NCT03106519

Liposome Bupivacaine for WRIST Blocks

Completed Phase 2 Last updated 10 September 2020
What this trial tests

Phase 2 trial testing Liposome bupivacaine + bupivacaine in Dupuytren's Contracture of the Hand (Viking's Disease) in 32 participants. Completed in 31 October 2017.

Timeline
2 January 2017
Primary endpoint
28 June 2017
31 October 2017

Quick facts

Lead sponsorCatherine Vandepitte, M.D.
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment32
Start date2 January 2017
Primary completion28 June 2017
Estimated completion31 October 2017
Sites1 location across Belgium

Drugs / interventions tested

Conditions studied

Sponsor

Catherine Vandepitte, M.D. — full company profile →

Who can join

Adults 18 to 85, any sex, with Dupuytren's Contracture of the Hand (Viking's Disease). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Treatment of Dupuytren's contracture requires multiple injections into the palm of the hand to weaken the cords, followed by rupture of the strands 2 days later. Anesthesia is required for both phases of treatment. It is hypothesized that extended-release liposome bupivacaine prolongs nerve blockade of the wrist allowing patients to undergo this 2-part regimen with less pain.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Effect of Bupivacaine Liposome Injectable Suspension on Sensory Blockade and Analgesia for Dupuytren Contracture Release.
    Vandepitte CF, Van Boxstael S, Duerinckx JF, Leunen I, et al · · 2019 · cited 7× · PMID 37470047 · DOI 10.1016/j.jhsg.2019.09.008

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