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evaluation of the effect of Novafen and Gelofen in post canal treatment pain decrement

Not Applicable
Conditions
Pharmacokinetics.
Other and unspecified diseases of pulp and periapical tissues
Registration Number
IRCT2014041316973N2
Lead Sponsor
Babol University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

1.The patient should be able to read , understand and complete the consent form; 2.Patient's consent form has been completed; 3.Teeth with a live pulp that do not have a peri-apical lesion should have been evaluated.
Exclusion criteria :
1.Pregnancy; 2.Hypersensitivity to NSAIDs and Sulfonamides; 3.History of asthma associated with nasal polyps; 4.History of chronic use of analgesics or sedatives; 5.Alcohol abuse; 6.Patients with uncontrolled hypertension; 7.Diabetes mellitus; 8.Renal disease, CNS disease, heart disease and liver dysfunction; 9.Cancer or major anomalies confirmed by clinical examinations or laboratory findings; 10.Aged less than 18 and more than 65; 11.Pregnancy or breastfeeding; 12.Analgesic use less than 12 hours to the beginning of the study.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: One hour before treatment. Method of measurement: 4,8,12,24,48.
Secondary Outcome Measures
NameTimeMethod
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