Third molar
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: To be included in the sample, patients will need to have the following characteristics: Display the indication for third molar extraction; Have a good general state of health that allows dental implant surgery; Have time and time available to attend dental appointments
Exclusion criteria
Exclusion criteria: Patients with any of the following characteristics may not be part of the sample: Patient with any systemic disease that prevents oral surgery; Patients who do not have time available for care.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary outcome - postoperative pain assessment After surgery, all patients will receive standardized postoperative care information and will be advised to take analgesics only when they deem it necessary. To assess postoperative pain, a visual analog scale (VAS) will be used. The EVA tool is a 10 cm ruler with 0 (no pain) at one end and 10 (severe pain) at the other, which will be given to patients after surgery. Patients will be asked to assess the worst level of pain they experienced within one week of surgery. In addition, patients will be instructed to record the duration of analgesic use in days. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary Outcome - Surgical Wound Healing On the day of suture removal, the surgical wound will be evaluated and classified as closed wound (first intention healing), open wound (second intention healing) or disorganized clot. All surgical complications will be recorded in the patient's record. | — |
Countries
Brazil
Contacts
Universidade Federal de Pelotas