NCT00519571

Evaluation of the Safety and Efficacy of Using ImplantLock Device - Dental Implant Accessory

• Status: Unknown
• Phase: N/A
• Study type: Interventional
• Enrollment: 15 (estimated)
• Sponsor: Innovative Implant Solutions · Industry
• Sex: All
• Age: 18 Years – 80 Years
• Healthy volunteers: Accepted

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.

Detailed 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.

Conditions

• Dental Implantation

Interventions

Type	Name	Description
DEVICE	ImplantLock device	dental implant

Timeline

• Start date: 2008-07-01
• Primary completion: 2009-06-01
• Completion: 2009-07-01
• First posted: 2007-08-22
• Last updated: 2008-05-09

Locations

1 site across 1 country: Israel