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Immediate Loading of Implants in Totally Edentate Upper and Lower Jaw. Trial to Evaluate Survival of the Implants and Bridges, Quality of Prosthetic Work and Patient Satisfaction
This study is currently recruiting participants.
Verified by University Hospital, Ghent, April 2009
First Received: September 6, 2005   Last Updated: April 7, 2009   History of Changes
Sponsored by: University Hospital, Ghent
Information provided by: University Hospital, Ghent
ClinicalTrials.gov Identifier: NCT00147992
  Purpose

This study is an evaluation of the survival of the implants and bridges, quality of prosthetic work and patient satisfaction after immediate loading of the implants in a totally edentate upper and lower jaw.


Condition Intervention
Dental Implants
Procedure: Immediate loading of implants in totally edentate upper and lower jaw

Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Active Control, Single Group Assignment, Efficacy Study
Official Title: Immediate Loading of Implants in Totally Edentate Upper and Lower Jaw. A Retrospective Trial to Evaluate Survival of the Implants and Bridges, Quality of Prosthetic Work and Patient Satisfaction

Further study details as provided by University Hospital, Ghent:

Primary Outcome Measures:
  • Survival of implants and bridges

Secondary Outcome Measures:
  • Quality of prosthetic work
  • Patient satisfaction

Estimated Enrollment: 50
Study Start Date: June 2005
Estimated Study Completion Date: December 2009
Estimated Primary Completion Date: December 2009 (Final data collection date for primary outcome measure)
Detailed Description:

This study is an evaluation of the survival of the implants and bridges, quality of prosthetic work and patient satisfaction after immediate loading of the implants in a totally edentate upper and lower jaw.

  Eligibility

Ages Eligible for Study:   18 Years to 90 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • 18-90 years old

Exclusion Criteria:

  • Medical risk patients
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00147992

Contacts
Contact: Hugo De Bruyn, MD, PhD + 32 9 332.40.18 hugo.debruyn@UGent.be

Locations
Belgium
University Hospital Ghent Recruiting
Ghent, Belgium, 9000
Contact: Bruno Collaert, MD     + 32 9 322.29.90     bruno.collaert@skynet.be    
Sponsors and Collaborators
University Hospital, Ghent
Investigators
Principal Investigator: Hugo De Bruyn, MD, PhD University Hospital, Ghent
  More Information

Additional Information:
No publications provided

Responsible Party: University Hospital Ghent ( Hugo De Bruyn )
Study ID Numbers: 2005/133
Study First Received: September 6, 2005
Last Updated: April 7, 2009
ClinicalTrials.gov Identifier: NCT00147992     History of Changes
Health Authority: Belgium: Institutional Review Board

ClinicalTrials.gov processed this record on September 04, 2009