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
Sponsors and collaborators
Armed Forces Institute of Dentistry, Pakistan
Lead sponsor
Armed Forces Post Graduate Medical Institute (AFPGMI), Rawalpindi
Sponsor institution