Study conducted in healthy human edentulous (toothless) that complete denture wearers with different types of artificial teeth to assess satisfaction, quality of life and chewing Total prosthesis
Conditions
Interventions
A double-blind crossover-controlled clinical trial with 60 elderly subjects will be conducted. The elderly will be divided into two groups: Group A (initially rehabilitated with functional teeth and,
Other
E06.780.346.760.300
Sponsors
Universidade Federal do Rio Grande do Norte
Universidade Federal do Rio Grande do Norte
Eligibility
Inclusion criteria
Inclusion criteria: Volunteers should be in good general health; both genders; absence of intraoral lesions and alteration of the perioral musculature detected by palpation; as well as signing the Free and Informed Consent Form. Edentulous individuals less than 5 years old will not be included in the sample.
Exclusion criteria
Exclusion criteria: Those who have given up part of the survey; were in poor health; unable to attend to where the search is performed.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome 1: efficient mastication of users of total dentures with anatomical and non-anatomical teeth evaluated by means of the sieve method. Expected outcome 2: satisfaction with total dentures with anatomical and non-anatomical teeth evaluated by means of a questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| ncreased quality of life verified by applying the OHIP-14 questionnaire, simplified version of the questionnaire Oral Healh Impact Profile. The final score will be evaluated to define the increase or decrease in the oral health impact on quality of life after the intervention. | — |
Countries
Brazil
Contacts
Public ContactAdriana Carreiro
Universidade Federal do Rio Grande do Norte
Outcome results
None listed