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NCT06108063

Mitigation of Arthrofibrosis After Total Knee Arthroplasty Using Losartan

Recruiting now Phase 1, PHASE2 Last updated 12 March 2024
What this trial tests

Phase 1, PHASE2 trial testing Losartan in Knee Arthroplasty, Total in 120 participants. Currently enrolling.

Timeline
6 March 2024
Primary endpoint
30 June 2027
30 June 2027

Quick facts

Lead sponsorSteadman Philippon Research Institute
PhasePhase 1, PHASE2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposeprevention
Enrollment120
Start date6 March 2024
Primary completion30 June 2027
Estimated completion30 June 2027
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Steadman Philippon Research Institute

Who can join

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

Sponsor's own description

The purpose of this study is to evaluate the efficacy of Losartan use post-operatively for reducing or preventing the development of arthrofibrosis and the associated adverse impacts on clinical outcomes.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Losartan

Trials testing the same drug.

Other recruiting trials for Knee Arthroplasty, Total

Currently open trials in the same condition.

Other Steadman Philippon Research Institute 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/NCT06108063.

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