Clinical Trials Directory

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UnknownNCT06161714

The Effectiveness of Buccal Infiltration Only Using Articaine for Extraction of Mandibular Molar

The Effectiveness of Buccal Infiltration Only Using Articaine for Routine Exodontia of Mandibular Molar: A Cross-Over Randomized Controlled Clinical Trial

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
Riyadh Elm University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The goal of this clinical trial, is to test out the efficacy of using Articaine only as a local anesthesia as buccal infiltration to extract lower molar teeth. Study will be performed in patients visiting Riyadh Elm University clinics seeking extraction of lower molars bilaterally, in each visit one molar tooth will be extracted using Ariticaine and the second visit with Lidocaine, pain level will be monitored and documented. This study may be helpful in providing scientific information to the oral maxillofacial surgeons which will assist them in choosing the best local anesthetic agent, and possibly substituting using inferior alveolar nerve block with infiltration only when extracting the mandibular posterior teeth.

Detailed description

This is a double-blind, randomized clinical trial, which will involve 40 patients visiting the out-patient department of Oral and Maxillofacial surgery. For each patient, one mandibular molar will be extracted from right as well as left side, with one side being anesthetized using 4% articaine with 1:100,000 epinephrine and other with 2% lidocaine with 1:100,000 epinephrine buccal infiltration only. Evaluation and comparison will be done on the basis of pain prevalence exhibited by the patients while extraction.

Conditions

Interventions

TypeNameDescription
DRUGArticaine 4%/Epi 1:100000 Inj Cart 1.7Ml4% articaine with 1:100,000 epinephrine buccal infiltration
DRUGLidocaine 2%/Epi 1:100000 Inj Cart 1.7Ml2% Lidocaine with 1:100,000 epinephrine buccal infiltration

Timeline

Start date
2023-11-30
Primary completion
2024-04-10
Completion
2024-04-30
First posted
2023-12-08
Last updated
2023-12-08

Source: ClinicalTrials.gov record NCT06161714. Inclusion in this directory is not an endorsement.