Pulpitis
Conditions
Interventions
Patients will be divided into 4 (four) groups, in a double-blind random choice, so that neither the patient nor the operator knows the solution to be used. In total, each group evaluated will have 45
Procedure/surgery
E06.397
Sponsors
Universidade Positivo
Universidade Positivo
Eligibility
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: Patients aged 18 to 75 years old; Indicative of endodontic treatment; biopulpectomy or necropulpectomy; Normal health conditions; Signed informed consent term.
Exclusion criteria
Exclusion criteria: Retreatment Immunocompromised patients (who make use of corticosteroids); Any known infectious diseases (e.g., HIV, hepatitis B, hepatitis C, tuberculosis); History of cancer within the oral-maxillofacial region; History of cancer in the last two years; History of radiotherapy of head and/or neck; non-odontogenic facial pain or patients with chronic pain; periodontal compromised tooth with mobility grade 2 or with a 6 mm periodontal pouch depth; teeth with incomplete rhizgenesis; Two adjacent teeth in direct contact subjected to root canal therapy; teeth with alterations that determine an increase in the preparation time (e.g., extreme morphologic changes or complications such as perforations, fractures and root calcifications ; Patients with allergy to Sodio Hypochlorite.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find as a primary result, after intervention in these groups, that patients have increased postoperative sensitivity in the group of teeth irrigated with NaOCl 8.25%, at least 5% in relation to the other groups. | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected as a secondary result, after the intervention, that the patients will not present sensitivity in the teeth that were irrigated with chlorhexidine, based on results already described in the literature. | — |
Countries
Brazil
Contacts
Public ContactLuciana Demenech
Universidade Positivo
Outcome results
None listed