Long-term Follow-up of the Anterior Lumbar Interbody Fusion Procedure.

NCT ID: NCT01666860

Last Updated: 2012-08-17

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

56 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-11-30

Study Completion Date

2011-07-31

Brief Summary

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During the period 1989-1999, a number of patients underwent an ALIF-procedure. Anterior Lumbar Interbody Fusion procedure (ALIF) is a type of lumbar spinal fusion. The approach of the lumbar region is by incision of the abdominal wall. The intervertebral disc is removed and replaced by a bone graft. These patients form the population of this study. The goal of this study is to evaluate their current medical condition and to determine the clinical outcome.

The clinical result will be stipulated by means of standardized questionnaires (VAS-score, Oswestry low Back Pain Questionnaire and SF-36)

Detailed Description

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Conditions

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Anterior Lumbar Interbody Fusion Procedure

Keywords

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anterior lumbar interbody fusion

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Anterior Lumbar Interbody Fusion procedure

Anterior Lumbar Interbody Fusion procedure

Intervention Type PROCEDURE

Interventions

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Anterior Lumbar Interbody Fusion procedure

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* An Anterior Lumbar Interbody Fusion procedure between 1999 and 2005

Exclusion Criteria

* None
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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Bart Poffyn, MD

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Ghent

Locations

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Ghent University Hospital

Ghent, , Belgium

Site Status

Countries

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Belgium

Related Links

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Other Identifiers

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2010/740

Identifier Type: -

Identifier Source: org_study_id