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.

First Received: August 26, 2005 Last Updated: December 19, 2007 History of Changes

Sponsors and Collaborators:	University Hospital, Ghent Institut Straumann AG
Information provided by:	University Hospital, Ghent
ClinicalTrials.gov Identifier:	NCT00137150

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

MedlinePlus related topics: Surgery

U.S. FDA Resources

Study Type:	Interventional
Study Design:	Treatment, Randomized, Open Label, Active Control, Single Group Assignment, Efficacy Study
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

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

Criteria

Inclusion Criteria:

18 years of age or older

Exclusion Criteria:

Smoking
Medical risk patients

Contacts and Locations

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

Website University Hospital Ghent This link exits the ClinicalTrials.gov site

No publications provided

Study ID Numbers:	2004/420
Study First Received:	August 26, 2005
Last Updated:	December 19, 2007
ClinicalTrials.gov Identifier:	NCT00137150 History of Changes
Health Authority:	Belgium: Institutional Review Board

ClinicalTrials.gov processed this record on May 07, 2009