Comparing Two different agents of Local anesthesia
- Conditions
- Health Condition 1: 3- Administration
- Registration Number
- CTRI/2024/01/061711
- Lead Sponsor
- Dr Rohan Jiteshkumar Doshi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 182
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.
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.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Effects of anesthesia with VRS scale and EPTTimepoint: 10 Minutes
- Secondary Outcome Measures
Name Time Method Requirement of additional anesthesia is Present or notTimepoint: 10 minutres