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NCT06087562

iPACK Block for Total Knee Arthroplasty

Status unknown Phase 4 Last updated 18 October 2023
What this trial tests

Phase 4 trial testing Ropivacaine 0.5% Injectable Solution 20mL in Knee Osteoarthritis in 350 participants. Status unknown.

Timeline
16 June 2020
Primary endpoint
30 September 2024
30 December 2024

Quick facts

Lead sponsorPoznan University of Medical Sciences
PhasePhase 4
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment350
Start date16 June 2020
Primary completion30 September 2024
Estimated completion30 December 2024
Sites1 location across Poland

Drugs / interventions tested

Conditions studied

Sponsor

Poznan University of Medical Sciences

Who can join

Adults 18 to 100, any sex, with Knee Osteoarthritis or Knee Pain Chronic. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This randomized, double-blinded, placebo-controlled trial seeks to evaluate the efficacy of the rehabilitation process of the Interspace between the Popliteal Artery and Capsule of the Posterior Knee (iPACK) block in total knee arthroplasty.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Knee Osteoarthritis

Currently open trials in the same condition.

Other Poznan University of Medical Sciences 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/NCT06087562.

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