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NCT01754363
Survivorship of Attune Primary Total Knee Prosthesis
NA trial testing Attune Primary Total Knee Replacement in Noninflammatory Degenerative Joint Disease in 1,542 participants. Participants enrolled and being followed up; not accepting new ones.
1 February 2030
Quick facts
| Lead sponsor | DePuy International |
|---|---|
| Phase | NA |
| Status | Active, enrolled |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 1,542 |
| Start date | 1 February 2013 |
| Primary completion | 1 February 2030 |
| Estimated completion | 1 February 2030 |
| Sites | 28 locations across Hong Kong, New Zealand, Malaysia, Belgium, Austria, United Kingdom, Germany, South Korea |
Drugs / interventions tested
- Attune Primary Total Knee Replacement
Conditions studied
- Noninflammatory Degenerative Joint Disease — all drugs for Noninflammatory Degenerative Joint Disease →
Sponsor
DePuy International — full company profile →
Who can join
Adults 22 to 75, any sex, with Noninflammatory Degenerative Joint Disease. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This post-marketing investigation will evaluate the long term (up to 15 years) survivorship of the Attune Primary Knee Prosthesis in patients with non-inflammatory degenerative joint disease. Data from Subjects who receive one of four knee configurations will be pooled to establish a contemporary dataset.
Publications & conference data
3 peer-reviewed publications reference this trial (live from Europe PMC):
-
Tibial Baseplate-Cement Interface Debonding in the ATTUNE Total Knee Arthroplasty System.
Torino D, Damsgaard C, Kolessar DJ, Hayes DS, et al · · 2022 · cited 20× · PMID 36164312 · DOI 10.1016/j.artd.2022.06.012 -
Learning curve with a new primary total knee arthroplasty implant: a multicenter perspective with more than 2000 patients.
Whittaker JP, Dwyer KA, Howard J, Huey V, et al · · 2018 · cited 7× · PMID 30186920 · DOI 10.1016/j.artd.2018.05.004 -
Comparison of Existing and New Total Knee Arthroplasty Implant Systems From the Same Manufacturer: A Prospective, Multicenter Study.
Hamilton WG, Brenkel IJ, Barnett SL, Allen PW, et al · · 2021 · cited 6× · PMID 34908561 · DOI 10.5435/jaaosglobal-d-21-00136
Verify or expand the search:
- PubMed search for NCT01754363
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other DePuy International trials
Trials by the same sponsor.
- NCT01635166 — Multi-centre Study to Assess the Long-term Performance of the Deltamotion Cup System in Primary Hip Replacement Surgery · Phase 4 · terminated
- NCT01418378 — Sigma CR150 Versus Sigma CR Knee RCT · Phase 4 · completed
- NCT01134445 — An Electronic Data Capture Study to Assess the Long-term Performance of the DePuy PROXIMA™ Hip in Primary Total Hip Repl · Phase 4 · terminated
- NCT00733499 — A Study to Determine the Difference in Low Contact Stress (LCS) Duofix Versus Low LCS Porocoat Knee Systems · NA · completed
- NCT00872573 — A Two Centre Study to Assess the Stability and Long-term Performance of the C-Stem™ AMT in a Total Primary Hip Replaceme · Phase 4 · terminated
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 NCT01754363 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 9 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by DePuy International
- Last refreshed: 14 April 2026
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/NCT01754363.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing