Maxillary implant overdentures retained by use of bars or locator attachments: 5-year findings from a randomized controlled trial.
Recruiting
- Conditions
- Complaints of maxillary prosthesis
- Registration Number
- NL-OMON21557
- Lead Sponsor
- one
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
Fully edentulous patients with complaints of their maxillary prosthesis, >18y/o, at least one year fully edentulous.
Exclusion Criteria
Previous preprosthetic surgery in maxilla, smoking, radiation therapy in head and neck region, medical contra-indications for surgery
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Peri-implant bone loss
- Secondary Outcome Measures
Name Time Method implant survival, changes in clinical (probing depth, modified bleeding index, gingiva index) parameters and patient satisfaction (validated questionnaires)