Clinical Trials Directory

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UnknownNCT06119139

Anesthetic Efficacy of 1.8 ml Versus 3.6 ml of 4% Articaine Buccal Infiltration

Anesthetic Efficacy of 1.8 ml Compared to 3.6 ml of Articaine Buccal Infiltration in Mandibular Molars With Symptomatic Irreversible Pulpitis: A Randomized Clinical Trial

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
70 (estimated)
Sponsor
Cairo University · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

The aim of the study is to compare the anesthetic efficacy and need for supplemental anesthesia of 1.8 ml compared to 3.6 ml of 4% articaine buccal infiltration in mandibular molars with symptomatic irreversible pulpitis.

Detailed description

Patients with moderate-to-severe pain due to symptomatic irreversible pulpitis will be included. Patients will be randomly assigned into two groups to receive either 1.8 ml 4% articaine buccal infiltration or 3.6. ml 4% articaine buccal infiltration before single visit root canal treatments. Intraoperative pain will be assessed using an 11-point numerical rating scale (NRS) so that anesthetic success will be defined as no to mild intraoperative pain. The need for supplemental anesthesia will also be recorded.

Conditions

Interventions

TypeNameDescription
DRUG3.6 ml 4% Articaine hydrochloride3.6 ml 4% articaine buccal infiltration
DRUG1.8 ml 4% Articaine hydrochloride1.8 ml 4% articaine buccal infiltration

Timeline

Start date
2023-12-01
Primary completion
2024-12-01
Completion
2025-06-01
First posted
2023-11-07
Last updated
2023-11-07

Source: ClinicalTrials.gov record NCT06119139. Inclusion in this directory is not an endorsement.