Post-operative pain, comfort.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Presentation of at least one residual root or indication of extraction; teeth severely destroyed by caries or fracture to the point of rendering their restoration unfeasible; prosthetic, periodontal or orthodontic indication; teeth of the jaw or jaw; incisors, canines and premolars; agree to participate in the study by signing the TCLE.
Exclusion criteria
Exclusion criteria: Patients with any factor that contraindicated the surgical act; infection installed on site; uncontrolled systemic disorders; diabetes and hypertension; problems in the coagulation cascade; severe anemia; allergies; patients who used some medicine with interference in bone metabolism; pregnant patients; patients who used drugs that stimulated gingival augmentation; asthmatic patients without the opinion of the pulmonologist; patients who had recently had Chikungunya; patients who were not involved in the planning of surgical and anesthetic techniques; not return to data collection; give up participating in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The patient's immediate pain level was 1.50 (SD: ± 1.98), level of pain patient comfort of 4.55 (SD: ± 0.90), level of satisfaction (SD: ± 1.12), pain level with 7 days post 0.73 (SD: ± 1.55) and comfort level with 7 days of 4.75 (SD: ± 0.74). | — |
Secondary
| Measure | Time frame |
|---|---|
| To describe the complications and limitations of the device during the surgical procedure and in the postoperative period with 7 days, and to mention to identify for which reasons they will occur. | — |
Countries
Brazil
Contacts
Universidade do Estado do Rio Grande do Norte