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NCT04092634

Dual Mobility in "High Risk" Patients

Active, enrolled Phase 4 Last updated 26 June 2025
What this trial tests

Phase 4 trial testing Dual mobility implant in Dislocation, Hip in 412 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
1 November 2017
Primary endpoint
1 June 2025
1 February 2035

Quick facts

Lead sponsorRush University Medical Center
PhasePhase 4
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment412
Start date1 November 2017
Primary completion1 June 2025
Estimated completion1 February 2035
Sites4 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Rush University Medical Center

Who can join

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

Sponsor's own description

The aim of this study is to compare clinical outcomes of patients considered to be high risk for prosthetic dislocation undergoing primary total hip arthroplasty (THA) with the use of a dual mobility bearing versus a conventional, single bearing design.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Rush University Medical Center trials

Trials by the same sponsor.

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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/NCT04092634.

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