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The SNAP trial: a double blind multi-center randomized controlled trial of a silicon nitride versus a PEEK cage in transforaminal lumbar interbody fusion in patients with symptomatic degenerative lumbar disc disorders: study protocol.
Kersten, Roel F M R; van Gaalen, Steven M; Arts, Mark P; Roes, Kit C B; de Gast, Arthur; Corbin, Terry P; Öner, F Cumhur.
Afiliação
  • Kersten RF; Clinical Orthopaedic Research Center-midden Nederland (CORC-mN), Department of Orthopaedics, Diakonessenhuis, Utrecht/Zeist, The Netherlands. rkersten@diakhuis.nl.
BMC Musculoskelet Disord ; 15: 57, 2014 Feb 25.
Article em En | MEDLINE | ID: mdl-24568365
ABSTRACT

BACKGROUND:

Polyetheretherketone (PEEK) cages have been widely used in the treatment of lumbar degenerative disc disorders, and show good clinical results. Still, complications such as subsidence and migration of the cage are frequently seen. A lack of osteointegration and fibrous tissues surrounding PEEK cages are held responsible. Ceramic implants made of silicon nitride show better biocompatible and osteoconductive qualities, and therefore are expected to lower complication rates and allow for better fusion.Purpose of this study is to show that fusion with the silicon nitride cage produces non-inferior results in outcome of the Roland Morris Disability Questionnaire at all follow-up time points as compared to the same procedure with PEEK cages. METHODS/

DESIGN:

This study is designed as a double blind multi-center randomized controlled trial with repeated measures analysis. 100 patients (18-75 years) presenting with symptomatic lumbar degenerative disorders unresponsive to at least 6 months of conservative treatment are included. Patients will be randomly assigned to a PEEK cage or a silicon nitride cage, and will undergo a transforaminal lumbar interbody fusion with pedicle screw fixation. Primary outcome measure is the functional improvement measured by the Roland Morris Disability Questionnaire. Secondary outcome parameters are the VAS leg, VAS back, SF-36, Likert scale, neurological outcome and radiographic assessment of fusion. After 1 year the fusion rate will be measured by radiograms and CT. Follow-up will be continued for 2 years. Patients and clinical observers who will perform the follow-up visits will be blinded for type of cage used during follow-up. Analyses of radiograms and CT will be performed independently by two experienced radiologists.

DISCUSSION:

In this study a PEEK cage will be compared with a silicon nitride cage in the treatment of symptomatic degenerative lumbar disc disorders. To our knowledge, this is the first randomized controlled trial in which the silicon nitride cage is compared with the PEEK cage in patients with symptomatic degenerative lumbar disc disorders. TRIAL REGISTRATION NCT01557829.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polietilenoglicóis / Fusão Vertebral / Materiais Biocompatíveis / Fixadores Internos / Dor Lombar / Compostos de Silício / Degeneração do Disco Intervertebral / Cetonas / Vértebras Lombares Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Aspecto: Patient_preference Limite: Adolescent / Adult / Aged / Humans / Middle aged Idioma: En Revista: BMC Musculoskelet Disord Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polietilenoglicóis / Fusão Vertebral / Materiais Biocompatíveis / Fixadores Internos / Dor Lombar / Compostos de Silício / Degeneração do Disco Intervertebral / Cetonas / Vértebras Lombares Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Aspecto: Patient_preference Limite: Adolescent / Adult / Aged / Humans / Middle aged Idioma: En Revista: BMC Musculoskelet Disord Ano de publicação: 2014 Tipo de documento: Article