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Evaluation of the Success Rate of Immediately Loaded Implants

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified December 2014 by University Hospital, Ghent.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT00314015
First Posted: April 12, 2006
Last Update Posted: December 5, 2014
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
University Hospital, Ghent
  Purpose

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 Intervention
Dental Implants Procedure: Evaluation of the success rate of implants Procedure: Questionnaires

Study Type: Interventional
Study Design: 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

Further study details as provided by University Hospital, Ghent:

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

Estimated Enrollment: 200
Study Start Date: January 2007
Estimated Study Completion Date: December 2015
Estimated Primary Completion Date: December 2015 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
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

  Eligibility

Information from the National Library of Medicine

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, Learn About Clinical Studies.


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
  Contacts and Locations
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
  More Information

Additional Information:
Responsible Party: University Hospital, Ghent
ClinicalTrials.gov Identifier: NCT00314015     History of Changes
Other Study ID Numbers: 2006/121
First Submitted: April 11, 2006
First Posted: April 12, 2006
Last Update Posted: December 5, 2014
Last Verified: December 2014