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Comparison of Outcome and Complications Encountered in Flapless Surgery and Immediate Loading Versus the Classical Surgical Approach and Loading After 6-8 Weeks in the Posterior Maxilla

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00137150
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.
Collaborator:
Institut Straumann AG
Information provided by:
University Hospital, Ghent
  Purpose
This study is a comparison of outcome and complications encountered in flapless surgery and immediate loading versus the classical surgical approach and loading after 6-8 weeks in the posterior maxilla.

Condition Intervention
Dental Implants Procedure: Placement of implants

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Comparison of Outcome and Complications Encountered in Flapless Surgery and Immediate Loading Versus the Classical Surgical Approach and Loading After 6-8 Weeks in the Posterior Maxilla

Further study details as provided by University Hospital, Ghent:

Primary Outcome Measures:
  • Implant survival at 6-12 months

Secondary Outcome Measures:
  • Prosthetic complications
  • Patient opinion

Estimated Enrollment: 15
Study Start Date: January 2005
Study Completion Date: September 2006
  Eligibility

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:

  • 18 years of age or older

Exclusion Criteria:

  • Smoking
  • Medical risk patients
  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): NCT00137150


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

Additional Information:
ClinicalTrials.gov Identifier: NCT00137150     History of Changes
Other Study ID Numbers: 2004/420
First Submitted: August 26, 2005
First Posted: August 29, 2005
Last Update Posted: December 28, 2007
Last Verified: December 2007