Immediate Load of Dental Implants, Placed in Atrophic Upper and/or Lower Jaw of Partial or Complete Edentate Patients, According to Flapless Technique

This study is currently recruiting participants.

Verified December 2011 by University Hospital, Ghent

First Received on August 25, 2005. Last Updated on December 30, 2011 History of Changes

Sponsor:	University Hospital, Ghent
Collaborator:	Nobel Biocare
Information provided by (Responsible Party):	University Hospital, Ghent
ClinicalTrials.gov Identifier:	NCT00136123

Purpose

This study will evaluate the placement of implants with minimal invasive techniques. Immediately after the placement of the implants, functional loaded synthetic teeth will be placed.

Condition	Intervention
Dental Implants	Procedure: Placement of functional loaded synthetic teeth after placement implants

Study Type:	Interventional
Study Design:	Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment
Official Title:	Immediate Load of Dental Implants, Placed in Atrophic Upper and/or Lower Jaw of Partial or Complete Edentate Patients, According to Flapless Technique

Further study details as provided by University Hospital, Ghent:

Primary Outcome Measures:

Implant success at 0-3 years [ Time Frame: At 0-3 years ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:

Prosthetic success [ Time Frame: At the moment ] [ Designated as safety issue: Yes ]
Patient opinion [ Time Frame: At same day ] [ Designated as safety issue: No ]

Estimated Enrollment:	20
Study Start Date:	December 2005
Estimated Study Completion Date:	December 2012
Estimated Primary Completion Date:	December 2012 (Final data collection date for primary outcome measure)

Intervention Details:

Placement of functional loaded synthetic teeth after placement implants

Eligibility

Ages Eligible for Study:	18 Years and older
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	Yes

Criteria

Inclusion Criteria:

18 years of age or older

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00136123

Contacts

Contact: Hugo De Bruyn, PhD	+ 32 9 332.40.18	hugo.debruyn@UGent.be
Contact: Hilde Browaeys	+ 32 9 332.40.21	hilde.browaeys@UGent.be

Locations

Belgium
University Hospital Ghent	Recruiting
Ghent, Belgium, 9000
Contact: Hilde Browaeys + 32 9 332.40.21 hilde.browaeys@UGent.be

Sponsors and Collaborators

University Hospital, Ghent

Nobel Biocare

Investigators

Principal Investigator:

Hugo De Bruyn, PhD

University Hospital, Ghent

More Information

Additional Information:

Website University Hospital Ghent This link exits the ClinicalTrials.gov site

No publications provided

Responsible Party:	University Hospital, Ghent
ClinicalTrials.gov Identifier:	NCT00136123 History of Changes
Other Study ID Numbers:	2005/218
Study First Received:	August 25, 2005
Last Updated:	December 30, 2011
Health Authority:	Belgium: Institutional Review Board

ClinicalTrials.gov processed this record on February 13, 2012