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Clinical Trials/IRCT201611242016N7
IRCT201611242016N7
Completed
未知

Compariosn of the combination of premedication with ibuprofen plus inferior alveolar block plus buccal infiltration with inferior alveolar block plus buccal infiltration on anesthesia success of posterior mandibular teeth with irreversible pulpitis: A three blinded randomized clinical trial

Vice Chancellor for Research and Technology0 sites100 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Irreversible Pulpitis.
Sponsor
Vice Chancellor for Research and Technology
Enrollment
100
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Vice Chancellor for Research and Technology

Eligibility Criteria

Inclusion Criteria

  • Age 18 or more than 18 years, no contraindications to taking either Ibuprofen (history of any allergic reaction to aspirin, NSAIDS, or Lidocaine with Epinephrine, nasal polyp, history of peptic ulcers or GI bleeding, pregnancy and lactation, renal or hepatic disease), no history of GI disorders or ulcer, having no serious systemic disease.
  • Exclusion criteria: no response to cold test, having sensitivity to percussion and palpation, having radiographic changes such as PDL widening, lack of vital pulp in coronal pulp chamber access cavity preparation, teeth with evidence of crack in their crown, having advanced periodontal disease, taking narcotic drugs or analgesic drugs in recent 24 hours before treatment.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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