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Effect of premedication on the depth of anesthesia during treatment of teeth diagnosed with irreversible pulpitis

Phase 2
Conditions
Irriversible pulpitis.
Irriversible pulpitis
Registration Number
IRCT201010094890N1
Lead Sponsor
Research deputy of Babol University of Medcial Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

patients with the signs and symptoms of irreversible pulpitis in a mandibular molar tooth. Exclusion criteria: presence of any systemic diseases; consumption of any analgesics for at least 12 hours before enrollment in the study; presence of any contraindication to take Ibuprofen , Gelfen, Acetaminophen or 2% lidocaine with 1:800,00 epinephrine, or injection teqniques; teeth with extended restorations; previous endodontic treatment; advanced periodontal disease and periapical Radiolucency.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Intensity of pain. Timepoint: before endodontic procedure, during access into dentin, when entering the pulp chamber. Method of measurement: Visual Analog Scale (VAS).
Secondary Outcome Measures
NameTimeMethod
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