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Immediate Load of Dental Implants, Placed in Atrophic Upper and/or Lower Jaw of Partial or Complete Edentate Patients, According to Flapless Technique

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ClinicalTrials.gov Identifier: NCT00136123
Recruitment Status : Unknown
Verified December 2014 by University Hospital, Ghent.
Recruitment status was:  Recruiting
First Posted : August 26, 2005
Last Update Posted : December 5, 2014
Sponsor:
Collaborator:
Nobel Biocare
Information provided by (Responsible Party):
University Hospital, Ghent

Brief Summary:
This study will evaluate the placement of implants with minimal invasive techniques. Immediately after the placement of the implants, functional loaded synthetic teeth will be placed.

Condition or disease Intervention/treatment Phase
Dental Implants Procedure: Placement of functional loaded synthetic teeth after placement implants Not Applicable

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 20 participants
Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Immediate Load of Dental Implants, Placed in Atrophic Upper and/or Lower Jaw of Partial or Complete Edentate Patients, According to Flapless Technique
Study Start Date : December 2005
Estimated Primary Completion Date : December 2015
Estimated Study Completion Date : December 2015

Arm Intervention/treatment
Experimental: Implants Procedure: Placement of functional loaded synthetic teeth after placement implants
Placement of functional loaded synthetic teeth after placement implants




Primary Outcome Measures :
  1. Implant success at 0-3 years [ Time Frame: At 0-3 years ]

Secondary Outcome Measures :
  1. Prosthetic success [ Time Frame: At the moment ]
  2. Patient opinion [ Time Frame: At same day ]


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

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): NCT00136123


Contacts
Contact: Hugo De Bruyn, PhD + 32 9 332.40.18 hugo.debruyn@UGent.be
Contact: Hilde Browaeys + 32 9 332.40.21 hilde.browaeys@UGent.be

Locations
Belgium
University Hospital Ghent Recruiting
Ghent, Belgium, 9000
Contact: Hilde Browaeys    + 32 9 332.40.21    hilde.browaeys@UGent.be   
Sponsors and Collaborators
University Hospital, Ghent
Nobel Biocare
Investigators
Principal Investigator: Hugo De Bruyn, PhD University Hospital, Ghent

Additional Information:
Responsible Party: University Hospital, Ghent
ClinicalTrials.gov Identifier: NCT00136123     History of Changes
Other Study ID Numbers: 2005/218
First Posted: August 26, 2005    Key Record Dates
Last Update Posted: December 5, 2014
Last Verified: December 2014