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Premedication efficacy of two oral analgesic on post root canal treatment pai

Phase 2
Conditions
Irreversible pulpitis.
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Z40-Z54
Registration Number
IRCT2015102916845N4
Lead Sponsor
Vice Chancellor for research of Dental Branch, Tehran Azad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

patients with age ranged 18-65; without systemic diseases ; without any medicine consumption; non smoking; non pregnant; non breast feeding; with asymptomatic irreversible pulpitis ( Visual Analog Scale(VAS) = 54); no allergies and hypersensitivity history to non-steroidal anti-inflammatory drugs and acetaminophen; need root canal treatment for a mandibular molar
Exclusion criteria: patients younger than 18 and older than 65; systemic diseases; any medicine consumption; pregnant and breast feeding;VAS more than 54; allergic history to drugs; normal pulp; no need to root canal treatment

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain after root canal treatment. Timepoint: 6,12,24 and 48 hour intervals. Method of measurement: Pain rate based on VAS.
Secondary Outcome Measures
NameTimeMethod
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