# A Retrospective Study to Evaluate the ConforMIS iTotal® Posterior Stabilized (PS) Knee Replacement System

> **NCT03289000** · — · COMPLETED · sponsor: **Restor3D** · enrollment: 93 (actual)

## Conditions studied

- Osteo Arthritis Knee

## Interventions

- **DEVICE:** iTotal Posterior Stabilized (PS) Knee Replacement System

## Key facts

- **NCT ID:** NCT03289000
- **Lead sponsor:** Restor3D
- **Sponsor class:** INDUSTRY
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2017-04-24
- **Primary completion:** 2017-08-04
- **Final completion:** 2017-12-31
- **Target enrollment:** 93 (ACTUAL)
- **Last updated:** 2023-10-25


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03289000

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03289000, "A Retrospective Study to Evaluate the ConforMIS iTotal® Posterior Stabilized (PS) Knee Replacement System". Retrieved via AI Analytics 2026-06-07 from https://api.ai-analytics.org/clinical/NCT03289000. Licensed CC0.

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