Evaluation of Implants Placed in the Regular Dentist's Practice

This study is currently recruiting participants. (see Contacts and Locations)
Verified January 2013 by University Hospital, Ghent
Sponsor:
Information provided by (Responsible Party):
University Hospital, Ghent
ClinicalTrials.gov Identifier:
NCT00286533
First received: February 1, 2006
Last updated: January 29, 2013
Last verified: January 2013
  Purpose

This study is an evaluation of the implants placed in a regular dentist's practice regarding:

  • gingiva condition
  • stability of implant
  • prothetic quality
  • questionnaires for the patients

Condition Intervention
Dental Implant
Procedure: Clinical examination (implant stability, gingiva condition, etc.)
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: Retrospective Evaluation of Implants Placed in the Regular Dentist's Practice. A Study to Evaluate Implant Success, Prosthetic Complications, Opinion of the Patient, and Quality of Care

Further study details as provided by University Hospital, Ghent:

Primary Outcome Measures:
  • gingiva condition [ Time Frame: t0 ] [ Designated as safety issue: No ]

Other Outcome Measures:
  • stability of implant [ Time Frame: t0 ] [ Designated as safety issue: No ]
  • prothetic quality [ Time Frame: t0 ] [ Designated as safety issue: No ]
  • questionnaires for the patients [ Time Frame: t0 ] [ Designated as safety issue: No ]

Estimated Enrollment: 500
Study Start Date: January 2006
Estimated Study Completion Date: December 2013
Estimated Primary Completion Date: December 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Placed implants Procedure: Clinical examination (implant stability, gingiva condition, etc.)
Clinical examination (implant stability, gingiva condition, etc.) to follow
Procedure: Questionnaires
Questionnaires are used.

  Eligibility

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

Inclusion Criteria:

  • Patients with implants placed in a regular dentist's practice
  Contacts and Locations
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, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00286533

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: NCT00286533     History of Changes
Other Study ID Numbers: 2005/414
Study First Received: February 1, 2006
Last Updated: January 29, 2013
Health Authority: Belgium: Institutional Review Board

Keywords provided by University Hospital, Ghent:
Implant

ClinicalTrials.gov processed this record on July 24, 2014