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A controlled clinical trial of implant-retained mandibular overdentures: clinical aspects.

Identifieur interne : 003E75 ( PubMed/Corpus ); précédent : 003E74; suivant : 003E76

A controlled clinical trial of implant-retained mandibular overdentures: clinical aspects.

Auteurs : E M Boerrigter ; R P Van Oort ; G M Raghoebar ; B. Stegenga ; P J Schoen ; G. Boering

Source :

RBID : pubmed:9131473

English descriptors

Abstract

In a controlled clinical trial, treatment effects of mandibular overdentures on two different implant-systems in edentulous patients were compared one year after insertion of the new dentures. The implant-systems used were the Brånemark system (Brå) and the IMZ-system. Treatment was randomly assigned to 60 patients according to a balanced allocation method. Evaluation included peri-implant and radiographical parameters. According to the Delphi method a clinical implant performance scale (CIP) was constructed based on all conceivable complications of the different implant systems. During the osseointegration period, five Brå- and one IMZ-implants were lost. The results of one of the peri-implant parameters and the radiographical score showed significant differences considering the (pseudo) pocket probing depth (Brå better than IMZ, P < 0.001) and the radiographic-score (IMZ better than Brå, P < 0.003). The results for the CIP-scale were less favourable for the Brå-group than for the IMZ-group; however, these differences were not significant.

PubMed: 9131473

Links to Exploration step

pubmed:9131473

Le document en format XML

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<name sortKey="Raghoebar, G M" sort="Raghoebar, G M" uniqKey="Raghoebar G" first="G M" last="Raghoebar">G M Raghoebar</name>
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<div type="abstract" xml:lang="en">In a controlled clinical trial, treatment effects of mandibular overdentures on two different implant-systems in edentulous patients were compared one year after insertion of the new dentures. The implant-systems used were the Brånemark system (Brå) and the IMZ-system. Treatment was randomly assigned to 60 patients according to a balanced allocation method. Evaluation included peri-implant and radiographical parameters. According to the Delphi method a clinical implant performance scale (CIP) was constructed based on all conceivable complications of the different implant systems. During the osseointegration period, five Brå- and one IMZ-implants were lost. The results of one of the peri-implant parameters and the radiographical score showed significant differences considering the (pseudo) pocket probing depth (Brå better than IMZ, P < 0.001) and the radiographic-score (IMZ better than Brå, P < 0.003). The results for the CIP-scale were less favourable for the Brå-group than for the IMZ-group; however, these differences were not significant.</div>
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