Clinical study to evaluate different adhesives in denture retentio

Not Applicable

Recruiting

• Conditions: Halitosis; Edentulism; Quality of Life; C23.888.821.475; C05.500.480; I01.800

• Registration Number: RBR-64gk7r
• Lead Sponsor: Faculdade de Odontologia de Ribeirão Preto da Universidade de São Paulo.

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-10-10
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Being clinically satisfactory users of total maxillary and mandibular prostheses (duration of prosthesis use is 1 year or less); properly understand both spoken and written Portuguese; be able to provide informed consent; being able to understand the study procedures and have the ability to perform them

Exclusion Criteria

Presence of oral mucosal lesions such as denture-induced fibrous hyperplasia, papillomas or traumatic ulcerations associated with prosthesis bases or prosthesis-related stomatitis;
Impaired cognitive function;
Inability to attend returns for evaluation and maintenance;
Patients on medications such as antibiotics, antifungals, immunosuppressants, anticoagulants and corticosteroids during the last 3 months prior to the survey.

Study & Design

• Study Type: Intervention
• Study Design: Not specified