Periapical Periodontitis
Conditions
Interventions
This is a randomized clinical study where a convenience sample will be used and the option for the type of intervention (number of sessions) will be defined during treatment. This study will be carrie
E06.397.778
Sponsors
Centro de Pesquisa da Universidade Positivo
Centro de Pesquisa da Universidade Positivo
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Both genders; older than 18 years; diagnosed with necrotic pulp; with normal physical and psychological health conditions; no use of analgesics and anti-inflammatories
Exclusion criteria
Exclusion criteria: Under 18 years old; vital pulp diagnosis; teeth with incomplete apex; pregnant; patients with non-odontogenic facial pain or chronic pain; patients who are taking analgesics and anti-inflammatories.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected Discharge 1 - It is expected to find a higher frequency of postoperative pain in endodontic treatments performed in multiple sessions, verify through a message sent to the cell phone of the research participants who will have to answer whether or not they had pain.;Outcome found 1 - It was observed that there was no significant difference for the presence of postoperative pain between treatments performed in single or multiple sessions (p=0.806), verified through information obtained from patients and statistical analysis of data. | — |
Secondary
| Measure | Time frame |
|---|---|
| Expected Discharge 2 -It is expected to find a greater intensity of postoperative pain in 24 hours after the completion of root canal treatment. Pain intensity will be verified through the Visual Analogue Scale (VAS), where the patient should give a score from zero to ten for pain. Zero, no pain, to ten, unbearable pain. Research participants will receive a message by cell phone, with the image of the Visual Analog Scale and will have to rate it according to the intensity of pain.;Outcome 2 - Pain was more intense in the first 24 hours both in the single session group (p<0.001) and in the multiple sessions group (p<0.001) compared to the other evaluated times, verified through the information obtained from the patients and statistical analysis of the data. | — |
Countries
Brazil
Contacts
Public ContactFlávia Tomazinho
Universidade Positivo
Outcome results
None listed