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anesthetic efficacy of 1.8 mL articaine, 1.8 mL and 3.6 mL of lidocaine for mental nerve block in irreversible pulpitis of the mandibular premolar

Not Applicable
Recruiting
Conditions
irreversible pulpitis of the mandibular premolar.
Pulpitis
K04.0
Registration Number
IRCT20210515051306N1
Lead Sponsor
Rafsanjan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
165
Inclusion Criteria

Healthy adult patients 18–60 years old
Having a mandibular premolar tooth with symptomatic irreversible pulpitis
Normal periapical radiographic appearance

Exclusion Criteria

History of sensitivity to 4%articaine or epinephrine
Systemic diseases
Pregnancy or breastfeeding
Any type of medication that could potentially interact with the anesthetic solution
Spontaneous pain
Periodontal disease or unable to get restoration
Having pain killer late 12 hours

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain score during treatment on Visual Analogue Scale (VAS). Timepoint: before administration of the anesthetic solution and during the endodontic treatment. Method of measurement: Visual Analogue Scale (VAS).
Secondary Outcome Measures
NameTimeMethod
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