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NCT03152357 · ClinicalTrials.gov registry record
A Retrospective Study to Evaluate the ConforMIS iUni, iDuo & iTotal® KRS
A clinical trial of Knee Osteoarthritis and Osteoarthritis, Knee, sponsored by Restor3D.
- Completed
- Registry status
- 950
- Enrollment target
- 1
- Study location
NCT03152357 is a study of Knee Osteoarthritis and Osteoarthritis, Knee that has completed, run by Restor3D. The registered enrollment target is 950 participants, above the 295-participant average among 101 other Knee Osteoarthritis trials with a reported enrollment target (222% higher). The trial reports 1 study location across 1 state.
The verdict
NCT03152357, a study of Knee Osteoarthritis and Osteoarthritis, Knee, has completed, sponsored by Restor3D.
- COMPLETED
- Registry status
- 950 participants
- Enrollment target
- 1
- Study location
Study Summary
This study is designed to evaluate implant survivorship, patient satisfaction, and patient-reported outcomes of subjects who have undergone surgery with any of the following ConforMIS knee implants: the iUni®, iDuo® or iTotal® Cruciate Retaining (CR) Knee Replacement Systems.
Conditions Studied
Interventions
- DEVICE ConforMIS iUni, iDuo, or iTotal (CR)
Study Locations (1)
Florida
- Preferred Orthopedics of the Palm Beaches - Boynton Beach
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 950 participants |
| Start Date | 2017-04-01 |
| Est. Completion | 2019-12-31 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03152357
The ClinicalTrials.gov registry entry for NCT03152357 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 950 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 295-participant average among 101 other Knee Osteoarthritis trials with a reported enrollment target (222% higher). The listed sponsor is Restor3D, which has 20 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Knee Osteoarthritis appearing as the primary indexed condition, and to 1 intervention - of which ConforMIS iUni, iDuo, or iTotal (CR) is the first listed.
NCT03152357 reports 1 study location spanning 1 distinct geographic area - top geographies include Florida.
Frequently Asked Questions
What is clinical trial NCT03152357 about?
NCT03152357 is a clinical study titled "A Retrospective Study to Evaluate the ConforMIS iUni, iDuo & iTotal® KRS". This study is designed to evaluate implant survivorship, patient satisfaction, and patient-reported outcomes of subjects who have undergone surgery with any of the following ConforMIS knee implants: the iUni®, iDuo® or iTotal® Cruciate Retaining (CR) Knee Replacement Systems.
What is the current status of trial NCT03152357?
This trial is currently completed. The enrollment target is 950 participants. The study started on 2017-04-01. Estimated completion is 2019-12-31.
What conditions does trial NCT03152357 study?
This clinical trial studies the following conditions: Knee Osteoarthritis, Osteoarthritis, Knee.
What interventions are being tested in trial NCT03152357?
The interventions under investigation include: ConforMIS iUni, iDuo, or iTotal (CR) (DEVICE).
Who is sponsoring clinical trial NCT03152357?
This trial is sponsored by Restor3D, which has 20 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03152357 being conducted?
This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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