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NCT02865447

Evaluation of Bone Mineral Density Changes After Total Hip Replacement: A Two-Year Clinical and DXA Analysis

Completed Last updated 2 August 2022
What this trial tests

trial testing total hip arthroplasty implant in Joint Disease in 25 participants. Completed in 24 August 2020.

Timeline
9 March 2017
Primary endpoint
24 August 2020
24 August 2020

Quick facts

Lead sponsorMicroPort Orthopedics Inc.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment25
Start date9 March 2017
Primary completion24 August 2020
Estimated completion24 August 2020
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

MicroPort Orthopedics Inc.

Who can join

Adults 21 to 80, any sex, with Joint Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Sponsor is conducting this post-market study to evaluate the clinical outcome and femoral bone mineral density (BMD) changes associated with the PROFEMUR® PRESERVE hip stem when used as indicated for primary total hip arthroplasty in patients with osteoarthritis of the hip joint.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Joint Disease

Currently open trials in the same condition.

Other MicroPort Orthopedics Inc. 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/NCT02865447.

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