Evaluation of the Success Rate of Immediately Loaded Implants

This study is currently recruiting participants.
Verified January 2013 by University Hospital, Ghent
Sponsor:
Information provided by (Responsible Party):
University Hospital, Ghent
ClinicalTrials.gov Identifier:
NCT00314015
First received: April 11, 2006
Last updated: January 29, 2013
Last verified: January 2013
  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
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: 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 ] [ Designated as safety issue: No ]
  • Prothetic complications [ Time Frame: Continuous follow-up ] [ Designated as safety issue: No ]
  • Opinion of the patient [ Time Frame: Continuous follow-up ] [ Designated as safety issue: No ]

Estimated Enrollment: 200
Study Start Date: January 2007
Estimated Study Completion Date: December 2013
Estimated Primary Completion Date: December 2013 (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

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Patients with immediately loaded implants
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: 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:
No publications provided

Responsible Party: University Hospital, Ghent
ClinicalTrials.gov Identifier: NCT00314015     History of Changes
Other Study ID Numbers: 2006/121
Study First Received: April 11, 2006
Last Updated: January 29, 2013
Health Authority: Belgium: Institutional Review Board

ClinicalTrials.gov processed this record on April 14, 2014