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NCT03152162

A Prospective Study to Evaluate the ConforMIS iTotal® (PS) Knee Replacement System

Terminated Last updated 25 October 2023
What this trial tests

trial testing iTotal PS KRS in Osteoarthritis, Knee in 102 participants. Terminated before completion.

Timeline
1 May 2017
Primary endpoint
1 November 2022
1 November 2022

Quick facts

Lead sponsorRestor3D
StatusTerminated
Study typeOBSERVATIONAL
Enrollment102
Start date1 May 2017
Primary completion1 November 2022
Estimated completion1 November 2022
Sites4 locations across United States

Drugs / interventions tested

Conditions studied

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 clinical study designed to observe the long-term clinical outcomes of total knee arthroplasty using a patient-specific, posterior stabilized implant in patients with osteoarthritis.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Osteoarthritis, Knee

Currently open trials in the same condition.

Other Restor3D 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/NCT03152162.

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