MedPath

The effect of two methods of using dexamethasone in reducing pain after root canal treatment

Phase 3
Conditions
Irreversible pulpitis.
Pulpitis
K04.0
Registration Number
IRCT20240109060657N1
Lead Sponsor
Boushehr University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
96
Inclusion Criteria

Male and female patients
Age over 18 years old
Vital pulp with a diagnosis of symptomatic or asymptomatic pulpitis
None of systemic diabetes and cardiovascular diseases and allergic problems
Willingness to cooperate
One-session root canal treatment
The possibility of achieving patency in all canals in preoperative radiography
Absence of periodontal problems

Exclusion Criteria

The complexity of the treatment and the possibility of prolonging the treatment time for more than 2 hours, which can be estimated from the patient's radiograph before starting the treatment.
History of gastric ulcer or gastrointestinal bleeding
History of allergy to NSAIDs or corticosteroids
Risk of renal failure or renal damage

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Average pain intensity. Timepoint: in the times before intervention, 3 hours after treatment, 6 hours, 12 hours, 24 hours after treatment. Method of measurement: NPRS ( Numeric Pain Rating Scale).
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath