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Outcome EnduRo Versus LINK SL Rotating Hinge Knee

NCT ID: NCT01952938

Last Updated: 2013-09-30

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

UNKNOWN

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-07-31

Brief Summary

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Randomized clinical outcome study of two rotating hinge knee prosthesis in knee surgery. Hypothesis: No difference in the clinical outcome for 1 year after the operation. Clinical follow-ups at 3, 10, 90 and 360 days after surgery. Measurement of clinical parameters

Detailed Description

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Conditions

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Knee Arthrosis,

Keywords

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knee revision surgery, rotating hinge prosthesis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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LINK SL

Patients

LINK SL versus EnduRo

Intervention Type PROCEDURE

EnduRo

Patients

LINK SL versus EnduRo

Intervention Type PROCEDURE

Interventions

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LINK SL versus EnduRo

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* rotating hinge knee indicated

Exclusion Criteria

* infection,
* malignant tumor,
* rheumatism
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Orthopaedische Klinik Koenig-Ludwig-Haus

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Orthopeadische Klinik KLH

Würzburg, Bavaria, Germany

Site Status RECRUITING

Countries

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Germany

Facility Contacts

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Maik Hoberg, MD

Role: primary

Other Identifiers

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AAG-I-H-1112

Identifier Type: -

Identifier Source: org_study_id