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NCT02865447
Evaluation of Bone Mineral Density Changes After Total Hip Replacement: A Two-Year Clinical and DXA Analysis
trial testing total hip arthroplasty implant in Joint Disease in 25 participants. Completed in 24 August 2020.
24 August 2020
Quick facts
| Lead sponsor | MicroPort Orthopedics Inc. |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 25 |
| Start date | 9 March 2017 |
| Primary completion | 24 August 2020 |
| Estimated completion | 24 August 2020 |
| Sites | 1 location across United States |
Drugs / interventions tested
- total hip arthroplasty implant
Conditions studied
- Joint Disease — all drugs for Joint Disease →
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.
Verify or expand the search:
- PubMed search for NCT02865447
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Joint Disease
Currently open trials in the same condition.
- NCT06713902 — Extracellular Vesicles in Fibrin Gel for Cartilage Repair · recruiting
- NCT04037735 — RSA-RCT: Attune S+ TKA Versus Sigma TKA · NA · recruiting
- NCT03865667 — Post Market Clinical Follow-Up Study Protocol for PROFEMUR® Preserve Femoral Stem · active not recruiting
Other MicroPort Orthopedics Inc. trials
Trials by the same sponsor.
- NCT07391592 — Post Market Clinical Follow-Up Study for EVOLUTION® NitrX™ Keeled Tibia and EVOLUTION® NitrX™ CS/CR Femur With Cruciate · active not recruiting
- NCT04147559 — Post Market Clinical Follow-Up Study for PROFEMUR® Preserve Classic Femoral Stem · enrolling by invitation
- NCT04145401 — Post Market Clinical Follow-Up Study- EVOLUTION® Revision CCK · enrolling by invitation
- NCT03865667 — Post Market Clinical Follow-Up Study Protocol for PROFEMUR® Preserve Femoral Stem · active not recruiting
- NCT03450733 — Wright Medical Technology Metal-on-Metal 522 Post-Market Surveillance Study · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT02865447 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by MicroPort Orthopedics Inc.
- Last refreshed: 2 August 2022
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