Comparison of three different root canal preparation instruments in the evaluation of post-treatment pain

Not Applicable

• Conditions: Health Condition 1: K040- Pulpitis

• Registration Number: CTRI/2023/01/049074
• Lead Sponsor: Kallepalli Meghana

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 26 June 2023

Recruitment & Eligibility

• Status: Closed to Recruitment of Participants
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1. Healthy adult patients based on ASA -1,2 requiring endodontic treatment in mandibular molars

2. Mandibular molars with symptomatic or asymptomatic irreversible pulpitis with or without apical periodontitis

3. Fully Formed roots

Exclusion Criteria

1. Patients with previous contributory medical history, pregnancy, and patients not defined as American Society of Anesthesiologists I

2. Patients under antibiotics, analgesics, or nonsteroidal anti-inflammatory drugs for the past 1 month

3. Mandibular molars with supernumerary roots

4. Presence of root canals with extreme canal curvature ( >30°)

Teeth with internal and external resorption, open apices

Presence of periapical pathosis, sinus tracts, and history of trauma

•Patients requiring endodontic retreatment

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Post instrumentation pain using VAS scaleTimepoint: 1st, 3rd and 7th day

Secondary Outcome Measures

Name	Time	Method
Post- instrumentation pain with respect to gender, pulp status and periapical diagnosis will be assessedTimepoint: 1st, 3rd and 7th day