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Follow-up of Patients After Knee Arthrodesis With an Intramedullary Nail

NCT ID: NCT00284297

Last Updated: 2022-12-20

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

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2005-09-30

Study Completion Date

2015-07-31

Brief Summary

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Follow-up of patients who underwent a knee arthrodesis with different types of intramedullary nails.

Detailed Description

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Conditions

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Knee Arthrodesis With Intramedullary Nail

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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knee arthrodesis

Group Type EXPERIMENTAL

History taken and clinical examination

Intervention Type PROCEDURE

History is taken and clinical examination is followed

Interventions

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History taken and clinical examination

History is taken and clinical examination is followed

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* All patients who underwent a knee arthrodesis with an intramedullary nail between 1994 and 2005

Exclusion Criteria

\-
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Ghent

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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René Verdonk, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Ghent

Locations

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University Hospital Ghent

Ghent, , Belgium

Site Status

Countries

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Belgium

Related Links

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http://www.uzgent.be

Website University Hospital Ghent

Other Identifiers

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2005/213

Identifier Type: -

Identifier Source: org_study_id