Quintex® Follow-up After One Year Minimum

NCT ID: NCT04489394

Last Updated: 2024-04-09

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

60 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-11-11

Study Completion Date

2020-02-18

Brief Summary

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Prospective study, not randomised, non-interventional, monocentric, investigating an intended patient cohort of 60 patients already operated on the cervical spine due to degenerative disc disease of the cervical spine down to the first thoracolumbar VBR (C2-T1), who received a Quintex plate for stabilisation

Detailed Description

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Conditions

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Degenerative Disc Disease Spondylolisthesis Trauma Spinal Stenosis Deformity of Spine Pseudoarthrosis of Spine Cervical Spondylosis Instability; Back

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

\- all patients who received a Quintex® Anterior Cervical Plate since 2014 until approx. end 2018 (minimum Follow-up is one year) in the study center

Exclusion Criteria

* Patient informed consent not signed
* Patients living outside a radius of 80 km around the study center
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Aesculap AG

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Katholisches Klinikum Koblenz

Koblenz, , Germany

Site Status

Countries

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Germany

References

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Bruchmann B, Kilian F. Follow-up of a new titanium cervical plate for fusion of the cervical spine. Orthop Rev (Pavia). 2023 Oct 12;15:84651. doi: 10.52965/001c.84651. eCollection 2023.

Reference Type RESULT
PMID: 37842541 (View on PubMed)

Other Identifiers

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AAG-O-H-1901

Identifier Type: -

Identifier Source: org_study_id

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