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ACTIVE NOT RECRUITING Phase 4

Dual Mobility in "High Risk" Patients

NCT04092634 · View on ClinicalTrials.gov ↗

Study Summary

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.

Conditions Studied

Interventions

  • DEVICE Dual mobility implant
  • DEVICE Traditional, Single-bearing hip implant

Study Locations (4)

California

  • Keck School of Medicine of USC — Los Angeles

Illinois

  • Rush University Medical Center — Chicago

New York

  • New York University Medical Center — New York

Pennsylvania

  • Rothman Orthopaedic Institute — Philadelphia

Trial Details

FieldValue
Enrollment Target 412 participants
Start Date 2017-11-01
Est. Completion 2035-02-01
Phase Phase 4

Sponsor

Rush University Medical Center

168 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04092634

The ClinicalTrials.gov registry entry for NCT04092634 describes a study currently listed as active not recruiting. It is categorized as Phase 4, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 412 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Rush University Medical Center, which has 168 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Dislocation, Hip appearing as the primary indexed condition, and to 2 interventions — of which Dual mobility implant is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT04092634 reports 4 study locations spanning 4 distinct geographic areas — top geographies include California, Illinois, New York. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT04092634 about?

NCT04092634 is a clinical study titled "Dual Mobility in "High Risk" Patients". 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.

What is the current status of trial NCT04092634?

This trial is currently active not recruiting. It is a Phase 4 study. The enrollment target is 412 participants. The study started on 2017-11-01. Estimated completion is 2035-02-01.

What conditions does trial NCT04092634 study?

This clinical trial studies the following conditions: Dislocation, Hip. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04092634?

The interventions under investigation include: Dual mobility implant (DEVICE), Traditional, Single-bearing hip implant (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04092634?

This trial is sponsored by Rush University Medical Center, which has 168 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04092634 being conducted?

This trial has 4 study locations across California, Illinois, New York, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial