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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

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ClinicalTrials.gov Identifier: NCT00147992
Recruitment Status : Unknown
Verified June 2015 by University Hospital, Ghent.
Recruitment status was:  Recruiting
First Posted : September 7, 2005
Last Update Posted : June 3, 2015
Sponsor:
Information provided by (Responsible Party):
University Hospital, Ghent

Brief Summary:
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 or disease Intervention/treatment
Dental Implants Procedure: Immediate loading of implants in totally edentate upper and lower jaw

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.

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 50 participants
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
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
Study Start Date : June 2005
Estimated Primary Completion Date : December 2015
Estimated Study Completion Date : December 2015

Arm Intervention/treatment
Experimental: implants Procedure: Immediate loading of implants in totally edentate upper and lower jaw
Immediate loading of implants in totally edentate upper and lower jaw.



Primary Outcome Measures :
  1. Survival of implants and bridges [ Time Frame: At beginning until last follow up ]

Secondary Outcome Measures :
  1. Quality of prosthetic work [ Time Frame: At end of follow up ]
  2. Patient satisfaction [ Time Frame: At end of follow up. ]


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 90 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • 18-90 years old

Exclusion Criteria:

  • Medical risk patients

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): 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

Additional Information:
Responsible Party: University Hospital, Ghent
ClinicalTrials.gov Identifier: NCT00147992     History of Changes
Other Study ID Numbers: 2005/133
First Posted: September 7, 2005    Key Record Dates
Last Update Posted: June 3, 2015
Last Verified: June 2015