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. (see Contacts and Locations)
Verified January 2013 by University Hospital, Ghent
Sponsor:
Collaborator:
Nobel Biocare
Information provided by (Responsible Party):
University Hospital, Ghent
ClinicalTrials.gov Identifier:
NCT00136123
First received: August 25, 2005
Last updated: January 29, 2013
Last verified: January 2013
  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 2013
Estimated Primary Completion Date: December 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Implants Procedure: Placement of functional loaded synthetic teeth after placement implants
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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

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:
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: January 29, 2013
Health Authority: Belgium: Institutional Review Board

ClinicalTrials.gov processed this record on September 16, 2014