Acute Pain. Loss of teeth due to accident, extraction or localized periodontal diseases
Conditions
Interventions
The sample will be based on 33 (trinta e três) patients according to the previously calculated sample, each one being included in 2 protocols, so that each patient has a protocol for each tooth on eac
PROTOCOL "B", surgical extraction using 2 placebo tablets + Real LED irradiation.
After asepsis, inferior alveolar nerve block and buccal nerve block, described by Malamed (Malamed, 2013), the techniq
Second evaluation: after 48h
Third evaluation: after 72h).
750 mg acetaminophen will be prescripted as a rescue analgesic in case of pain and the patient should note if it was
Device
Procedure/surgery
E02.774
E02.594.540
Sponsors
Departamento de Odontologia da Universidade Federal de Sergipe
Universidade Federal de Sergipe
Eligibility
Age
18 Years to 30 Years
Inclusion criteria
Inclusion criteria: ASA I or II patients who have extraction of 3rd molars indication with the same anchor position according to the classification of Pell and Gregory. Aged between eighteen and thirty years.
Exclusion criteria
Exclusion criteria: ASA III and IV Patients. Presence of periodontal problem. Use of antidepressants of any kind. Parafunctional habits. Smokers. History of hypersensitivity reaction to the LED (LED). History of previous pericoronarite. Odontophobic. Individuals under the age of eighteen or over the age of thirty. Diabetics
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected Outcome 1: It is expected that there will be control of postoperative pain from the observation of a variation of at least 5% in the sites irradiated with the LED, and the measurement will be done by the patient in the form delivered by the researcher, who counts on the Analog Visual Scale (AVE), where 0 represents absence of pain and 10 represents unbearable pain. Data were collected twenty-four, forty-eight and seventy-two hours after the intervention. | — |
Secondary
| Measure | Time frame |
|---|---|
| Expected Outcome 1: It is expected that the measurement of the visual analogue scale does not exceed 5cm and, in protocol B, equivalent to or less than protocol A from the observation of a variation of at least 5% | — |
Countries
Brazil
Contacts
Public ContactAgnaldo Prata Júnior
Universidade Federal de Sergipe
Outcome results
None listed