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

NCT01397617 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 177

Last updated 2016-04-22

Study results available
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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.

Conditions

  • Partial Edentulism
  • Complete Edentulism

Interventions

DEVICE

NobelActive Internal implant

Dental implant

DEVICE

NobelActive External implant

Dental implant

DEVICE

NobelReplace Tapered Groovy implant

Dental implant

Sponsors & Collaborators

  • Nobel Biocare

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-04-30
Primary Completion
2013-05-31
Completion
2013-05-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01397617 on ClinicalTrials.gov