Evaluation of the benefit of different doses of dipyrone in third molar surgery

Phase 4

• Conditions: Tooth not erupted; A14.549.167.860.715

• Registration Number: RBR-26frc3
• Lead Sponsor: niversidade de Pernambuco

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-10-10
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruitment completed
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Healthy patients aged between 18 and 35, thus patients who did not present systemic alterations nor used continuous medication. The lower third molars should have the same angulation (mesio-angular, rectangular, vertical or horizontal), similar root formation, and the same degree of impact as Pell and Gregory classification. The teeth should be impacted. The patient should also not have pericoronitis within the last 30 days before surgery, and the region could not have signs of inflammation.

Exclusion Criteria

Patients who did not agree to participate in the study after reading the consent form; had an allergy to the medicines used; did not fit the planning of surgical and anesthetic techniques; had a history of haematological disease or gastrointestinal bleeding; pregnant and lactating women; smokers; did not return to the second surgery (surgery on the opposite side); used other medications in the postoperative period; postoperative infection; difference greater than 10 minutes between the surgical times of the operated sides.

Study & Design

• Study Type: Intervention
• Study Design: Not specified