Skip to content

Comparing Two different agents of Local anesthesia

Comparative evaluation of Only buccal infiltration of 4% Articaine verses Buccal and palatal infiltration of 2% Lignocaine in patients with Symptomatic irreversible pulpitis in maxillary molars: A Randomized clinical study - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/01/061711
Enrollment
182
Registered
2024-01-22
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: 3- Administration

Interventions

Intervention1: 4% Articaine: Only Buccal Infiltration of 4% articaine in maxillary molars with symptomatic irreversible pulpitis. Anesthesia effect will be last for 3 hours approx. Control Interventio

Sponsors

Dr Rohan Jiteshkumar Doshi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Systemically healthy both male and female patients between 18-60 years of age will be included in the study. 2. Patients diagnosed with symptomatic irreversible pulpitis with or without apical periodontitis giving prolonged response to cold test in maxillary molars. 3. Patient should have actively experienced moderate to severe pain pre operatively on VAS scale above 4 is included in the study 4. A written informed consent will be taken from all the patients and only those patients ready to sign the consent form will be included in the study.

Exclusion criteria

Exclusion criteria: 1. Patients allergic to local anesthetics or known allergy to Lignocaine and articaine will be excluded from study. 2. Pregnant and lactating patients will be excluded from study. 3. Patients taking any analgesics, antibiotics, sedatives, and antianxiety drugs on regular basis or before 24 hrs.of treatment will be excluded. 4. Patient having necrosed tooth with sinus tracts/local gum swelling around the affected tooth. 5. Patients with severe periodontitis and poor oral hygiene will be excluded from the study.

Design outcomes

Primary

MeasureTime frame
Effects of anesthesia with VRS scale and EPTTimepoint: 10 Minutes

Secondary

MeasureTime frame
Requirement of additional anesthesia is Present or notTimepoint: 10 minutres

Countries

India

Contacts

Public ContactDr Rohan Jiteshkumar Doshi

Sumandeep Vidhyapeeth

nshah7873@gmail.com9998994299

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026