IRCT20210515051306N2CompletedUnknown
Comparative evaluation of anesthetic efficacy of 1.8 mL articaine and 3.6 mL of articaine for mental nerve block in mandibular premolars with irreversible pulpitis: A randomized clinical trial study
Conditions
Trial Snapshot
- Phase
- Unknown
- Status
- Completed
- Enrollment
- 64
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 years to 60 years (—)
- Sex
- All
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
Investigators
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