Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT04849884 · ClinicalTrials.gov registry record · NA
To Evaluate the Performance of the CORI™ KNEE TENSIONER as an Accessory to the CORI™ Surgical System.
A NA study of Arthroplasty and Replacement, sponsored by Smith & Nephew.
- Active
- Registry status
- NA
- Development phase
- 50
- Enrollment target
- 4
- Study locations
NCT04849884 is a NA study of Arthroplasty and Replacement that is active but no longer recruiting, run by Smith & Nephew. The registered enrollment target is 50 participants, below the 231-participant average among 5 other Arthroplasty trials with a reported enrollment target (78% lower). The trial reports 4 study locations across 4 states.
The verdict
NCT04849884, a NA study of Arthroplasty and Replacement, is active but no longer recruiting, sponsored by Smith & Nephew.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
- 4
- Study locations
Study Summary
To evaluate the performance of the CORI™ KNEE TENSIONER as an accessory to the CORI™ Surgical System.
Conditions Studied
Interventions
- DEVICE CORI™ KNEE TENSIONER
Study Locations (4)
New York
- Hospital for Special Surgery - New York
Ohio
- OrthoNeuro - New Albany
Pennsylvania
- University of Pittsburgh, Magee - Pittsburgh
Wisconsin
- Memorial Medical Center - Ashland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2022-02-10 |
| Est. Completion | 2026-04-30 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04849884
The ClinicalTrials.gov registry entry for NCT04849884 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 231-participant average among 5 other Arthroplasty trials with a reported enrollment target (78% lower). The listed sponsor is Smith & Nephew, which has 72 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Arthroplasty appearing as the primary indexed condition, and to 1 intervention - of which CORI™ KNEE TENSIONER is the first listed.
NCT04849884 reports 4 study locations spanning 4 distinct geographic areas - top geographies include New York, Ohio, Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT04849884 about?
NCT04849884 is a clinical study titled "To Evaluate the Performance of the CORI™ KNEE TENSIONER as an Accessory to the CORI™ Surgical System.". To evaluate the performance of the CORI™ KNEE TENSIONER as an accessory to the CORI™ Surgical System.
What is the current status of trial NCT04849884?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2022-02-10. Estimated completion is 2026-04-30.
What conditions does trial NCT04849884 study?
This clinical trial studies the following conditions: Arthroplasty, Replacement, Knee.
What interventions are being tested in trial NCT04849884?
The interventions under investigation include: CORI™ KNEE TENSIONER (DEVICE).
Who is sponsoring clinical trial NCT04849884?
This trial is sponsored by Smith & Nephew, which has 72 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04849884 being conducted?
This trial has 4 study locations across New York, Ohio, Pennsylvania, Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Arthroplasty
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
-
INHANCE Stemless Reverse Shoulder IDE
RECRUITING · NA
-
Healthy Living After Knee Replacement
ACTIVE NOT RECRUITING · NA
-
Triathlon Tritanium Cone Augments Outcomes Study
ACTIVE NOT RECRUITING · NA
-
Continuous Adductor Canal Block (CACB) vs. Combined Spinal Epidural (CSE) in Total Knee Arthroplasty
COMPLETED · NA
-
Dilute Betadine Lavage in the Prevention of Postoperative Infection
COMPLETED · Phase 4
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.