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Evaluation the effect of the Lornoxicam on the post-operative endodontic pai

Phase 2
Conditions
Post operative endodontic pain.
Other specified disorders of teeth and supporting structures
Registration Number
IRCT201108017191N1
Lead Sponsor
Dental Azad University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
40
Inclusion Criteria

healthy (ASA I, II); Patients with first or second mandibular molars who need endodontic treatment; Vital tooth without a history of past endodontic treatment; Patients with clinical evidence of irreversible Pulpits with moderate to severe pain; Patients without pre apical lesion and periodontal ligament enlargement more than 0.75-1mm on the x-ray images; Patients in the age group of 18-65 years old. Exclusion criteria: Pregnant or nursing; necrotic tooth; Patients with allergy or contraindication toward non-opioid or opioid painkillers such as aspirin or NSAIDs; People who have a history of acute peptic ulcer, during the past 12 months; People who have bleeding problems or have been taking anticoagulant drugs over the past month; Patients who have taken opioid or non opioid or steroid pain killers, antidepressants or sedative drugs.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Post oprative endodontic pain. Timepoint: 6-12-24-48 hours after treatment. Method of measurement: Visual Analogue Scale (VAS 0-9mm).
Secondary Outcome Measures
NameTimeMethod
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