Comparison of anesthetic effectiveness and safety of 2% lidocaine and 4% articaine for mandibular third molar impaction surgery †A randomized control trial study

Phase 2

Completed

• Conditions: Duration of anesthesiaOnset of anesthesiaCardiovascular changeVisual analog scaleParesthesia; Efficacy; Articaine; Lidocaine; Mandibular third molar impaction; Randomized; Clinical

• Registration Number: TCTR20201218003
• Lead Sponsor: /A

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2020-12-14
• Study Start: 2020-12-18
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 68

Inclusion Criteria

1.Patients with mesioangular positioned depth B lower third molar impaction
2.Absence of systemic illness(ASA I)
3.Age between 18 to 40 years old
4.Provided written informed consent
5.communicated with Thai language

Exclusion Criteria

1.Patient has any signs of inflammation or infection at the extraction site
2.Pregnancy or current lactation
3.Take any other pain medication prior to the removal of third molar
4.History of allergic reaction of local anesthesia
5.History of bleeding tendency or was given any anticoagulant drugs

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Duration of anesthesia at the beginning of placing the incision measured from time of placing the incision to the last suture placed,Onset of anesthesia at the beginning of injection recorded from time of injection of the onset of anesthesia of the lower lip,Cardiovascular change at the beginning of procedure recorded before procedure, during injection, placing the incision and sectioning of tooth ,Visual analog scale at the end of treatment Intra operatively pain was scored by patient,Paresthesia at the day of suture removal observed any signs of paresthesia clinically

Secondary Outcome Measures

Name	Time	Method
/A N/A N/A