Evaluation of the use of Analgesic Medication before Surgery to reduce Anxiety in patients who will undergo Wisdom Teeth Extraction: clinical, double-blind, randomized trial
Not Applicable
Recruiting
- Conditions
- Fear of Dental TreatmentF03.950.750.500
- Registration Number
- RBR-3vskx79
- Lead Sponsor
- niversidade Estadual de Ponta Grossa
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
Young patients, between 20 and 40 years old; Both genders; ASA I and II (specific anamnesis questionnaire); Patients who need the removal of a lower third molar that requires making a surgical flap and osteotomy; Absence of signs and symptoms of infection at the site to be operated on; Accept to participate and sign the Informed Consent Form (TCLE).
Exclusion Criteria
Allergy or history of allergy to any medication; Patients who are pregnant or breastfeeding; Patients using antidepressant medication or other central nervous system depressants; Any contraindication for the use of opioids associated with paracetamol; Patients with active infection at the surgical site.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method It is expected to find a reduction in patients' levels of anxiety, pain and complaints with the use of preemptive analgesic medication, using the evaluation method through applied questionnaires where we will observe a reduction or not in the patient's stress levels.
- Secondary Outcome Measures
Name Time Method It is expected to find that the use of medication improves the perception of the surgical procedure for the patient during the trans-surgical moment, by reducing the levels of trans-operative pain, through the application of questionnaires, where we will observe a reduction in levels of patient pain during surgery.