Ellipse Intramedullary High Tibial Osteotomy Nail Study

NCT ID: NCT02519218

Last Updated: 2018-02-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

6 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-08-31

Study Completion Date

2017-12-31

Brief Summary

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The purpose of this study is to collect outcomes data in patients implanted with the Ellipse IM HTO Nail System.

Detailed Description

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Conditions

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Osteoarthritis Varus Malalignment

Study Design

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Observational Model Type

COHORT

Study Time Perspective

OTHER

Interventions

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Ellipse Technologies Intramedullary High Tibial Osteotomy Nail System

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Patient implanted with the Ellipse IM HTO Nail System for osteoarthritis and varus malalignment of the knee
* Patient signs informed consent for the use of their personal private data.

Exclusion Criteria

* Patient is currently enrolled in another clinical trial for high tibial osteotomy.
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ellipse Technologies, Inc.

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Mark Dahl, MD

Role: PRINCIPAL_INVESTIGATOR

University of Minnesota

Other Identifiers

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PR0179

Identifier Type: -

Identifier Source: org_study_id

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