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Impact of overdentures retained by a single mandibular implant on the swallowing threshold, quality of life and speech of edentulous elderly

Not Applicable
Conditions
Elderly
Denture
Speech
Deglutition
Quality of life
Dental Implantation.
F01.145.209.908.677
M01.060.116.100
E06.780.346.760.290
Registration Number
RBR-47gbn4
Lead Sponsor
niversidade Estadual de Campinas- Faculdade de Odontologia de Piracicaba
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruitment completed
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

It will be selected 18 elderly over 60 years old, according to the following inclusion criteria: to be totally edentulous in the upper and lower dental arches, and to use upper and lower dentures for at least 1 year; to have posterior mandibular alveolar process sharply reabsorbed, with height less than or equal to 15 mm³,and lower anterior alveolar ridge compatible with the implant, and with a minimum bone volume of 8 mm, condition detected after radiographic examination and / or tomographic; to be a Portuguese native speaker and finally to be literate.

Exclusion Criteria

The elderly with parafunctional habits; craniofacial malformation; moderate to deep hearing loss (evaluated by tonal audiometry), which are users or not of any individual sound amplification apparatus; cognitive impairment (evaluated through the application of the Mini Mental State Examination) ; aged with some language disorder; aged with severe speech disorder; elderly already done laryngeal surgery; aged who had experience with speech evaluations and with psychophysical; elderly with symptoms of temporomandibular joints and / or chewing muscles; aged with uncontrolled systemic diseases; neurological diseases, such as: ischemic or hemorrhagic stroke, traumatic brain injury, Parkinson's disease, Alzheimer's disease; elderly with psychiatric disorders which change the articulation of speech and the course of this study; smokers; alcoholics; aged who have performed head and / or neck irradiation due oncological diseases will be eliminated of this study.

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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