Comparison of Anesthetic Efficacy OF 2% Lidocaine Inferior Alveolar Nerve (IANB) Block Versus Primary Buccal Infilteration With 4% Articaine in Symptomatic Irreversible Pulpitis(SIP) IN Mandibular First Molars

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-55
SponsorArmed Forces Institute of Dentistry, Pakistan

About this trial

This randomized controlled trial aims to compare the anesthetic efficacy of 2% lignocaine administered through an inferior alveolar nerve block (IANB) in one group of participants with 4% articaine delivered via primary buccal infiltration in other group in patients with symptomatic irreversible pulpitis in mandibular first molars.

Eligibility criteria

Qualifiers

Systemically healthy patients classified as ASA I, aged 18-55 years.

Permanent mandibular first molar tooth requiring endodontic therapy.

Diagnosed with symptomatic irreversible pulpitis without swelling or sinus.

Normal periapical radiographic appearance (no evidence of periapical pathology).

Disqualifiers

• Pregnant or lactating mothers.

Teeth with reversible pulpitis, previously treated, or with calcified canals.

Teeth with severe periodontal disease or periapical radiolucency.

Patients who have taken analgesics or anti-inflammatory drugs within 6 hours before the treatment visit.

Trial design

Treatments tested in this trial

  • INTERVENTION 1: 2% Lignocaine 1:80,000 epinephrine
  • INTERVENTION 2 : 4%Articaine 1:100,000 epinephrine

Treatment groups

330 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Armed Forces Institute of Dentistry, Pakistan

Lead sponsor

Armed Forces Post Graduate Medical Institute (AFPGMI), Rawalpindi

Sponsor institution