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

> **NCT03152162** · — · TERMINATED · sponsor: **Restor3D** · enrollment: 102 (actual)

## Conditions studied

- Osteoarthritis, Knee

## Interventions

- **DEVICE:** iTotal PS KRS

## Key facts

- **NCT ID:** NCT03152162
- **Lead sponsor:** Restor3D
- **Sponsor class:** INDUSTRY
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** TERMINATED
- **Start date:** 2017-05-01
- **Primary completion:** 2022-11-01
- **Final completion:** 2022-11-01
- **Target enrollment:** 102 (ACTUAL)
- **Why stopped:** Decision of investigational team
- **Last updated:** 2023-10-25


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03152162

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03152162, "A Prospective Study to Evaluate the ConforMIS iTotal® (PS) Knee Replacement System". Retrieved via AI Analytics 2026-06-07 from https://api.ai-analytics.org/clinical/NCT03152162. Licensed CC0.

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