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Evaluation of the Success Rate of Immediately Loaded Implants

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ClinicalTrials.gov Identifier: NCT00314015
Recruitment Status : Unknown
Verified December 2014 by University Hospital, Ghent.
Recruitment status was:  Recruiting
First Posted : April 12, 2006
Last Update Posted : December 5, 2014
Sponsor:
Information provided by (Responsible Party):
University Hospital, Ghent

Brief Summary:

Evaluation of the success rate of immediately loaded implants based on:

  • condition of the gingiva
  • stability of the implants
  • evaluation of the RXs
  • questionnaires

Condition or disease Intervention/treatment Phase
Dental Implants Procedure: Evaluation of the success rate of implants Procedure: Questionnaires Not Applicable

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 200 participants
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Evaluation of the Success Rate of Immediately Loaded Implants
Study Start Date : January 2007
Estimated Primary Completion Date : December 2015
Estimated Study Completion Date : December 2015

Arm Intervention/treatment
Experimental: Patients with immediately loaded implants. Procedure: Evaluation of the success rate of implants
Evaluation of the success rate of implants will be followed.
Procedure: Questionnaires
Questionnaires will be used



Primary Outcome Measures :
  1. Success of implants [ Time Frame: Continuous follow-up ]
  2. Prothetic complications [ Time Frame: Continuous follow-up ]
  3. Opinion of the patient [ Time Frame: Continuous follow-up ]


Information from the National Library of Medicine

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

Inclusion Criteria:

  • Patients with immediately loaded implants

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): NCT00314015


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: Hugo De Bruyn, MD, PhD    + 32 9 332.40.18    hugo.debruyn@UGent.be   
Principal Investigator: Hugo De Bruyn, MD, PhD         
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: NCT00314015     History of Changes
Other Study ID Numbers: 2006/121
First Posted: April 12, 2006    Key Record Dates
Last Update Posted: December 5, 2014
Last Verified: December 2014