ight emitting diode (LED) action in the Pain control ater wisdom teeth Extractio
Not Applicable
- Conditions
- Acute Pain. Loss of teeth due to accident, extraction or localized periodontal diseasesR52.0K08.1
- Registration Number
- RBR-5fr3qm
- Lead Sponsor
- Departamento de Odontologia da Universidade Federal de Sergipe
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruitment completed
- Sex
- Not specified
- Target Recruitment
- Not specified
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
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
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method 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%<br>