Localized Alveolar Ridge Augmentation With Space Maintenance Devices

TerminatedOBSERVATIONAL
Enrollment

10

Participants

Timeline

Start Date

October 31, 2009

Primary Completion Date

March 31, 2011

Study Completion Date

March 31, 2011

Conditions
Alveolar Bone Loss
Interventions
DEVICE

INFUSE® Bone Graft

Patients will be treated with the commercially available INFUSE® Bone Graft material applied to an ACS concurrent with space maintenance devices for soft tissue management on Day 0 (Surgery). A follow-up visit will take place 2 weeks after implant of the INFUSE® Bone Graft material, or as regularly scheduled as per the standard of care (SOC) for the facility. Patients will return to the facility for final End of Study (EOS) assessments approximately 6 months after surgery. Between the follow-up visit and the EOS visit, patients will be seen as per the SOC schedule for the facility.

Trial Locations (8)

28037

Denver

34237

Sarasota

47904

Lafayette

60611

Chicago

80111

Greenwood Village

90049

Los Angeles

90095

Los Angeles

97221

Portland

Sponsors
All Listed Sponsors
collaborator

Averion International Corporation

INDUSTRY

lead

Medtronic Spinal and Biologics

INDUSTRY

NCT00991432 - Localized Alveolar Ridge Augmentation With Space Maintenance Devices | Biotech Hunter | Biotech Hunter