# A Single Time-Point Study to Evaluate the ConforMIS iTotal® (CR) Knee Versus Off-the-Shelf

> **NCT02251522** · — · COMPLETED · sponsor: **Restor3D** · enrollment: 873 (actual)

## Conditions studied

- Osteoarthritis

## Interventions

- **DEVICE:** ConforMIS Total Knee Replacement System
- **DEVICE:** Off-the-Shelf Knee Replacement System

## Key facts

- **NCT ID:** NCT02251522
- **Lead sponsor:** Restor3D
- **Sponsor class:** INDUSTRY
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2014-10
- **Primary completion:** 2016-10
- **Final completion:** 2016-12
- **Target enrollment:** 873 (ACTUAL)
- **Last updated:** 2023-10-25


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02251522

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02251522, "A Single Time-Point Study to Evaluate the ConforMIS iTotal® (CR) Knee Versus Off-the-Shelf". Retrieved via AI Analytics 2026-06-08 from https://api.ai-analytics.org/clinical/NCT02251522. Licensed CC0.

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