Skip to content

Assessing the Wear Rates of the ADM/MDM Hips Using 3D X-ray Analysis

Assessing the Wear Rates of the ADM/MDM Dual Mobility Hips Manufactured by Stryker Orthopaedics Using 3D X-ray Analysis

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04019925
Enrollment
120
Registered
2019-07-15
Start date
2019-09-01
Completion date
2020-08-31
Last updated
2019-07-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arthroplasty, Replacement, Hip

Brief summary

A common complication post hip replacement is hip dislocation or hip instability which can lead to the hip implants being revised. A new generation of Dual Mobility hips was designed to minimize hip dislocation/hip instability and polyethylene wear thus increasing the longevity of the hip prosthesis and reducing the number of re-operations for a patient. In this study we will be assessing 2 dual mobility hips manufactured by Stryker Orthopaedics Inc. The ADM and the MDM.

Detailed description

Hip replacement is a procedure in which the hip joint is replaced by a prosthetic implant or prosthesis. Post op hip dislocation or hip instability is a common complication which can lead to the hip implants being revised. There are many types of hip prostheses manufactured with the aim of prolonging longevity of the prosthesis and minimizing postoperative complications. One of these is a new generation of dual mobility hip manufactured by Stryker Orthopaedics. The Anatomic Dual Mobility (ADM) and the Modular Dual Mobility (MDM) were designed to minimize hip dislocation/hip instability and polyethylene wear thus increasing the longevity of the hip prosthesis and reducing the number of re-operations for a patient. In this study we will be assessing the outcome of the ADM and MDM hip system.

Interventions

DEVICEADM/MDM hip

Dual Mobility Hip prosthesis manufactured by Stryker Orthopaedics: ADM/MDM

Sponsors

Stryker Orthopaedics
CollaboratorINDUSTRY
Unity Health Toronto
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Male or non-pregnant female * Skeletally mature * 18 to 75 years old * Stryker Dual Mobility Hip prosthesis * BMI between 20 and 35 * Follow-up x-rays between 3 years and 6 years postop

Exclusion criteria

* Dual Mobility Hip implant that is not the ADM or MDM * BMI that is 19 or less * BMI that is greater than 36 * Most recent x-rays less than 3 years postop

Design outcomes

Primary

MeasureTime frameDescription
To assess the change in polyethylene wear of Dual Mobility hip implants using Stryker Orthopaedics ADM & MDM prosthesesbefore the patient's discharge home, 6 weeks postop, and the most recent x-ray taken up to 5 years postop.This study will assess the change in linear and volumetric wear using 3D x-ray analysis. Measurements will be taken of x-rays obtained before the patient's discharge home, 6 weeks postop, and the most recent x-ray taken more than 3 years postop.

Secondary

MeasureTime frameDescription
To review the number of postop hip dislocations/hip instabilitiesfirst 5 years post surgeryDislocations and the post op time for each occurrence per patient will be collected in tabular format. This in turn will be used to calculate percent of cases/subject.

Countries

Canada

Contacts

Primary ContactKerry Ann K. Griffith-Cunningham
griffithk@smh.ca416 864-6060

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026