Stomatitis, Denture
Conditions
Interventions
This is a randomized, controlled, double-blind, single-center, two-arm clinical study. Neither the researchers who will evaluate the outcomes nor the statistical analyst will be aware of which group e
2. After washing it well with running water and mild soap
and 3. At night (sleeping period) remove the denture and place i
Sponsors
Faculdade de Odontologia da Universidade Federal de Goiás
Universidade Federal de Goiás
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients using upper total dentures (PT) with a clinical diagnosis of Denture Stomatitis; over 18 years old; both sexes; with autonomy and ability to understand the purpose of the treatment and availability to voluntarily collaborate with the research
Exclusion criteria
Exclusion criteria: Patients allergic to any component of the DOCTIVE® formulation; immunocompromised; who have recently made continuous use of systemic or topical intraoral antifungals; patients who have recently made use of broad-spectrum antibiotics
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find improvement or worsening of the signs and symptoms of Denture Stomatitis | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate the cost-effectiveness of Doctive® compared to the use of nystatin in the treatment of Denture Stomatitis | — |
Countries
Brazil
Contacts
Public ContactNádia do Lago Costa
Universidade Federal de Goiás
Outcome results
None listed