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Clinical Trials/IRCT2015103124798N1
IRCT2015103124798N1Completed未知

Effect of dexamethasone as a supplemental buccal infiltration of the posterior teeth after an inferior alveolar nerve block (lidocaine 2% with 0.00001 epinephrine), on during and post treatment pain, in patients with symptomatic irreversible pulpitis

Vice Chancellor for research of Islamic Azad University Isfahan (Khorasgan)0 sites60 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
60

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
74 years to 43 years (—)
Sex
All

Inclusion Criteria

  • lack of medication to work. Tooth in response to cold and electrical tests have long-term positive response and radiographic signs of the presence of radiolucent not have any. During vital pulp coronal access cavity preparation should be there. Exclusion criteria: pregnancy or lactation, age less than 18 years, having any kind of infectious disease or endocrine disease, moderate to advanced periodontal disease, tooth non-living, allergy to dexamethasone

Exclusion Criteria

  • Not provided

Investigators

Sponsor
Vice Chancellor for research of Islamic Azad University Isfahan (Khorasgan)

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