Dental Hyperesthesia
Conditions
Interventions
Patients with dental hyperesthesia as evidenced by clinical history, underwent one minute, antiseptic mouth rinsing with clorhexidine 0,2%, the operative mouth field is set, the tooth surface is dried
Chlorhexidine
Sponsors
Center of Biomaterials of Havana University
Eligibility
Sex/Gender
All
Age
20 Years to 75 Years
Inclusion criteria
Inclusion criteria: Patients older than 20 years old and younger than 75 years old with dental hyperesthesia who consented to participate in the clinical trial
Exclusion criteria
Exclusion criteria: Patients with malignant neoplasia in areas close to the site of treatment. Patients with mental incapacity and/or severe psychological disorders Pregnant or breastfeeding women Patients with allergic reactions to gentian violet or acrylics Patients with uncontrolled diabetes Patients with alcoholism or other drugs addictions Patients that do not consent to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain relief, 48 hours, 96 hours, 5 days, 6 days No adverse reactions, up to 6 days | — |
Secondary
| Measure | Time frame |
|---|---|
| Irritation of oral mucosa around the site after the application of the product, 48 hours, 96 hours, 5 days, 6 days. Warmth on treated area, 48 hours, 96 hours, 5 days, 6 days. | — |
Countries
Cuba
Contacts
Public ContactRosa Guerra Bretaña
Center of Biomaterials of Havana University
Outcome results
None listed