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The Mini-Screw as Orthodontic Anchoring: Survival, Clinical Efficiency and Experience of the Patient

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00137137
First Posted: August 29, 2005
Last Update Posted: December 28, 2007
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:
University Hospital, Ghent
  Purpose
This is a clinical trial to evaluate the mini-screw as orthodontic anchoring. This trial will study implant survival, clinical efficiency and experience of the patient.

Condition Intervention
Dental Implants Procedure: Placement of the mini-screw

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: The Mini-Screw as Orthodontic Anchoring: A Clinical Trial to Study Survival, Clinical Efficiency and Experience of the Patient

Further study details as provided by University Hospital, Ghent:

Primary Outcome Measures:
  • Implant survival

Secondary Outcome Measures:
  • Patient opinion
  • Efficacy of treatment

Estimated Enrollment: 20
Study Start Date: June 2005
Study Completion Date: November 2006
  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:   10 Years to 70 Years   (Child, Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • 10-70 years of age
  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): NCT00137137


Locations
Belgium
University Hospital Ghent
Ghent, Belgium, 9000
Sponsors and Collaborators
University Hospital, Ghent
Investigators
Principal Investigator: Hugo De Bruyn, PhD University Hospital, Ghent
  More Information

Additional Information:
ClinicalTrials.gov Identifier: NCT00137137     History of Changes
Other Study ID Numbers: 2005/097
First Submitted: August 26, 2005
First Posted: August 29, 2005
Last Update Posted: December 28, 2007
Last Verified: December 2007