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NCT04667559
A Study to Evaluate the Conformis iTotal Identity Knee Replacement System
trial testing Conformis iTotal Identity Knee Replacement System in Osteoarthritis, Knee in 22 participants. Terminated before completion.
14 December 2022
Quick facts
| Lead sponsor | Restor3D |
|---|---|
| Status | Terminated |
| Study type | OBSERVATIONAL |
| Enrollment | 22 |
| Start date | 12 October 2020 |
| Primary completion | 14 December 2022 |
| Estimated completion | 14 December 2022 |
| Sites | 2 locations across United States |
Drugs / interventions tested
- Conformis iTotal Identity Knee Replacement System
Conditions studied
- Osteoarthritis, Knee — all drugs for Osteoarthritis, Knee →
Sponsor
Restor3D
Who can join
18 and older, any sex, with Osteoarthritis, Knee. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This is a prospective multicenter study located in the United States. Subjects will be implanted with an iTotal Identity Knee Replacement System and followed for 10 years post implantation.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT04667559
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Osteoarthritis, Knee
Currently open trials in the same condition.
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- NCT06488144 — Rehabilitation for Arthritis of The Knee: mainTaining Improvement for Veterans · Phase 3 · recruiting
- NCT07386561 — Virtual Reality Therapy and Non-Sleep Deep Rest Relaxation After Joint Arthroplasty · NA · active not recruiting
- NCT07514598 — Effect of J-Shaped Incision After Total Knee Arthroplasty (J-TKA) · NA · active not recruiting
- NCT07058623 — Nurse-Led Telehealth vs In-Person Follow-Up After Total Knee Replacement · NA · recruiting
Other Restor3D trials
Trials by the same sponsor.
- NCT05231304 — Retrospective Evaluation of Clinical and Radiographic Outcomes Following Total Talus Replacement · completed
- NCT05114356 — Cervical Interbody Fusion Device Patient Registry · terminated
- NCT04180423 — TKA Operating Room Efficiency for TKA Using Customized Implant Techniques · terminated
- NCT03738462 — A Study to Evaluate the Conformis Hip System · terminated
- NCT03289754 — A Prospective Study to Evaluate the iTotal Knee and iPoly XE Tibial Inserts · NA · 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 NCT04667559 (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 Restor3D
- Last refreshed: 25 October 2023
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/NCT04667559.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing