RecruitingEarly Phase 1NCT07108465

Comparative Experimental Study Between Bupivacaine and Ropivacaine Regarding Efficacy in Third Molar Removal Surgery Under General Anesthesia


Sponsor

Henrique Tedesco

Enrollment

15 participants

Start Date

Jul 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this clinical trial is to compare the efficacy of bupivacaine and ropivacaine in third molar removal surgery under general anesthesia in healthy volunteers. The main question aims to determine whether there is any difference in vital signs, hemostasis and postoperative pain between ropivacaine and bupivacaine in patients undergoing third molars extraction under general anesthesia. Researchers will compare bupivacaine and ropivacaine in a split-mouth study to determine if one drug is more effective in third molar extraction surgery under general anesthesia (better hemostasis, less postoperative pain, and fewer changes in vital signs). Participants will undergo a single surgical procedure and complete the Visual Analog Scale to record postoperative pain


Eligibility

Min Age: 18 YearsMax Age: 60 Years

Inclusion Criteria3

  • Patients aged 18 to 60
  • Patients ASA Physical Status Classification I and II
  • Patients with impacted or semi-impacted lower third molars with similar positioning on both sides according to the Pell and Gregory classification

Exclusion Criteria2

  • Patients who can have surgery under local anesthesia
  • Patients where more procedures are required in the same surgical session

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Interventions

DRUGBupivacaine 0,5%

Injection of bupivacaine 0,5% in group A

DRUGRopivacaine 0,75%

Injection of ropivacaine 0,75% in group B


Locations(1)

Hospital de Clínicas de Porto Alegre

Porto Alegre, Rio Grande do Sul, Brazil

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NCT07108465


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