Dental Pulp Necrosis
Conditions
Interventions
The children will be divided into two groups: test group (40 deciduous molars treated with CTZ) and control group (40 deciduous molars treated with 3Mix-MP). Both folders will be manipulated respectin
Drug
Sponsors
Universidade Federal de Alagoas
Universidade Federal de Alagoas
Eligibility
Inclusion criteria
Inclusion criteria: Children previously authorized by their parents to take part in the study through the Informed Consent Term (TCLE); Children aged 6 to 7 years; Children with satisfactory systemic health and who do not use continuous systemic medication for the treatment of acute or chronic diseases; Children who do not have any type of syndrome; Children who have at least one non-vital deciduous molar;
Exclusion criteria
Exclusion criteria: Non-restorable deciduous molars or perforation on the pulp floor;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess the occurrence of pain by anamnesis (pain recordatoy) at intervals of 1, 6 and 12 months after initial allocated treatment. Data will be described in numbers and percentages as reported by the existence or persistence of pain after intervention. | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate the remission or appearance of fistulas and abscesses by intraoral physical examination at intervals of 1.6 and 12 months after initial treatment. Data will be described using event numbers.;To evaluate percussion sensitivity by intraoral physical examination at intervals of 1, 6, and 12 months after initial treatment. Data will be described by numbers and percentages and according to the report of acute and severe pain after percussion.;To evaluate physiological mobility on palpation by intraoral physical examination at intervals of 1, 6 and 12 months after initial treatment. Mobilities greater than 1 mm will be considered non-physiological. Data will be described in numbers and percentages.;Radiographically, cases will be considered successful when the size of periapical or interradicular radiolescence reduces or does not increase in size when compared with the radiograph of the initial examination. Data will be collected at intervals of 1.6, 12 months after initial treatment. Data will be described in number and percentage. | — |
Countries
Brazil
Contacts
Public ContactValdeci Santos
Universidade de Pernambuco
Outcome results
None listed