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Clinical Trial Summary

To investigate the safety and effectiveness of the ImplantLock device and its contribution to 8.0 mm long root-form endosseous implants stability under immediately applied continuous functional loading.


Clinical Trial Description

Primary Endpoints

- Serious adverse events occurrence rate (during implantation procedure or following implantation) related to the ImplantLock device will be documented in Serious Adverse Event Form.

- Adverse events occurrence rate (during implantation procedure or following implantation) related to the ImplantLock device will be documented in Adverse Event Form.

Secondary Endpoints

- Determine 8.0 mm long endosseous implant stability while using ImplantLock Device. Stability will be routinely assessed.

- Determine the ability to immediately apply continuous functional loading on 8.0 mm long endosseous implant while using ImplantLock Device. The ability to immediately apply continuous functional loading will be routinely assessed. ;


Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00519571
Study type Interventional
Source Innovative Implant Solutions
Contact Hanna Levy, Dr
Phone 972-4-638-8837
Email hanna@qsitemed.com
Status Not yet recruiting
Phase N/A
Start date July 2008
Completion date July 2009

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