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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

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ClinicalTrials.gov Identifier: NCT00137150
Recruitment Status : Completed
First Posted : August 29, 2005
Last Update Posted : December 28, 2007
Sponsor:
Collaborator:
Institut Straumann AG
Information provided by:
University Hospital, Ghent

Study Description
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Brief Summary:
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 or disease Intervention/treatment Phase
Dental Implants Procedure: Placement of implants Not Applicable

Study Design
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Study Type : Interventional  (Clinical Trial)
Enrollment : 15 participants
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
Study Start Date : January 2005
Actual Study Completion Date : September 2006
Arms and Interventions
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Outcome Measures
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Primary Outcome Measures :
  1. Implant survival at 6-12 months

Secondary Outcome Measures :
  1. Prosthetic complications
  2. Patient opinion

Eligibility Criteria
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Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
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
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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
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Belgium
University Hospital Ghent
Ghent, Belgium, 9000
Sponsors and Collaborators
University Hospital, Ghent
Institut Straumann AG
Investigators
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Principal Investigator: Hugo De Bruyn, PhD University Hospital, Ghent
More Information
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Additional Information:

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ClinicalTrials.gov Identifier: NCT00137150    
Other Study ID Numbers: 2004/420
First Posted: August 29, 2005    Key Record Dates
Last Update Posted: December 28, 2007
Last Verified: December 2007