Position HTO Multicenter NIS

NCT ID: NCT00889304

Last Updated: 2011-07-22

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

221 participants

Study Classification

OBSERVATIONAL

Study Start Date

2007-07-31

Study Completion Date

2010-06-30

Brief Summary

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Evaluation of the Position HTO system in patients with unicompartmental medial arthrosis after open wedge high tibial osteotomy

Detailed Description

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Conditions

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Medial Monocompartmental Osteoarthritis of the Knee

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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A

HTO cohort

Position HTO system

Intervention Type DEVICE

open wedge high tibial osteotomy

Interventions

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Position HTO system

open wedge high tibial osteotomy

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

Exclusion: Clinically relevant disorders of bone metabolism, Aktive infection, Adipositas (BMI ≥ 35), Rheumatoid arthritis, Osteomyelitis in the tibia, No availibility for follow-up examinations
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Aesculap AG

INDUSTRY

Sponsor Role lead

Responsible Party

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Aesculap AG

Principal Investigators

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Jürgen Fritz, Dr.

Role: PRINCIPAL_INVESTIGATOR

Winghofer Medicum

Locations

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Orthopädie Harthausen

Bad Aibling, , Germany

Site Status

Caritas-Krankenhaus Bad Mergentheim

Bad Mergentheim, , Germany

Site Status

Universitätsklinikum Regensburg

Regensburg, , Germany

Site Status

Winghofer Medicum

Rottenburg, , Germany

Site Status

BGU Tübingen

Tübingen, , Germany

Site Status

Countries

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Germany

Other Identifiers

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AAG-O-H-0702

Identifier Type: -

Identifier Source: org_study_id

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