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Clinical Trials/CTRI/2024/03/064923
CTRI/2024/03/064923
Not yet recruiting
Phase 4

Effectiveness of oral premedication on anesthetic success of Inferior alveolar nerve block in mandibular molars with symptomatic irreversible pulpitis using Dexamethasone and combination of Dexamethasone and Ibuprofen A double blinded randomized controlled trial - NI

Poojamol P V0 sites0 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
Poojamol P V
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Poojamol P V

Eligibility Criteria

Inclusion Criteria

  • Healthy adult patients aged 18 to 45 years
  • Presence of irreversible pulpitis with moderate to severe pain in mandibular molars, without any
  • signs of periapical involvement.
  • Patients not taken analgesics for at least 12 hours before enrollment in the study

Exclusion Criteria

  • Patients with allergies and hypersensitivity to medications, local anesthetic solution, or its
  • Pregnant or nursing women
  • Immunocompromised patients
  • Patients with active sites of pathosis in the area of injection

Outcomes

Primary Outcomes

Not specified

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