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Randomized, Open Investigation Evaluating the Efficacy of Nobel Biocare SFB and CFB Implants

Partial Edentulism Clinical Trial

Official title:
Evaluation of NobelBiocare SFB and CFB Implants

Clinical Trial Summary

The purpose of this study is to determine the survival rate, marginal bone resorption, soft tissue health and maintenance of the NobelActive Internal and External implants and to make comparisons with the NobelReplace Tapered Groovy implant placed in healed sites.

Clinical Trial Description

The purpose of this study is to determine safety and efficacy parameters for the NobelActive Internal and External implants and to make comparisons with the NobelReplace Tapered Groovy implant placed in healed sites.

Safety: AEs

Efficacy:

- survival rates,

- marginal bone resorption with marginal bone levels measurement,

- soft tissue health and maintenance via gingival index measurement, plaque index, papilla index . ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01397617
Study type Interventional
Source Nobel Biocare
Contact
Status Completed
Phase N/A
Start date April 2006
Completion date September 2014
View Details
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