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An Open Prospective Study to Evaluate the Survival Rate and Marginal Bone Response of Astra Tech Dental Implants, Fixture ST, in Patients With Tooth Loss in the Posterior Maxilla.
The purpose of this study is primarily to evaluate implant survival rate of Astra Tech Fixture ST placed in the posterior maxilla. A one-stage surgical protocol will be used and the implants will be loaded four weeks after implant installation (early loading). Marginal bone levels, plaque and status of the periimplant mucosa will also be evaluated. The subjects will be followed for three years.
Age
18 - 75 years
Sex
ALL
Healthy Volunteers
No
Dept. of Periodontology, New York Dept of Veterans Affairs Medical Center
New York, New York, United States
Dept. of Prosthodontics, New York Dept of Veterans Affairs Medical Center
New York, New York, United States
Start Date
September 1, 2000
Primary Completion Date
August 1, 2008
Last Updated
February 15, 2012
19
ACTUAL participants
Astra Tech Fixture ST
DEVICE
Lead Sponsor
Dentsply Sirona Implants and Consumables
NCT02814149
NCT05315414
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT05883202