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Comparative evaluation of the effect of ibuprofen lysine & gelofen - acetaminophen on pai

Phase 2
Recruiting
Conditions
Irreversible pulpitis.
Pulpitis
K04.0
Registration Number
IRCT20140527017880N8
Lead Sponsor
Kermanshah University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

Candidates for Root thtapy
Age over 12 years
Ability to read and understand the visual analog scale

Exclusion Criteria

Useof other anti pain drug befor treatment
Cystic teeth
Hopless teeth
sensitivity to the drugs present in the study
Age under 12 years
liver problems
history of chemotherapy
Heart problems
Kidney disease
Stomach problem

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: 8,16,24 and 48 hour after treatment. Method of measurement: visual analog scale.
Secondary Outcome Measures
NameTimeMethod
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