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Clinical Trials/IRCT2016083129618N2
IRCT2016083129618N2CompletedPhase 2

Comparison of the Effects Pre treatment with Acetaminophen and Ibuprofen in Inferior Alveolar Nerve Block of Second Primary Molar Teeth with Irreversible Pulpitis

Vice Chancellor for Research, Tabriz University of Medical Sciences0 sites30 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Phase 2
Status
Completed
Sponsor
Enrollment
30

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
6 years to 8 years (—)
Sex
All

Inclusion Criteria

  • children with no history of allergy to Acetaminophen and Ibuprofen; allergy to 2% Lidocaine Anesthetic drugs with 1/200000 epinephrine; no record of intraoral injection; having no unpleasant experience of medical record; phobia from dentistry and no use of analgesic agents during the previous 24 hours periods; mandibular second primary molar with irreversible pulpits without alveolar abscess.
  • Exclusion criteria: systemic diseases; allergy to lidocaine with 1/200000 epinephrine; allergy to anti-inflammatory nonsteroidal drugs peptic ulcer and use of any pain- killer 24 hours before treatment.

Exclusion Criteria

  • Not provided

Investigators

Sponsor
Vice Chancellor for Research, Tabriz University of Medical Sciences

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