A clinical study on post operative pain after single sitting root canal treatment.

Not Applicable

Conditions: Health Condition 1: K040- Pulpitis

Registration Number: CTRI/2023/07/054831

Lead Sponsor: MGM Dental College and Hospital

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: ot Yet Recruiting

Sex: Not specified

Target Recruitment: 0

Inclusion Criteria

1.All vital single-rooted teeth with irreversible pulpitis, whether associated with or without apical periodontitis, and mild to moderate pain (VAS value 5-74mm) indicated root canal treatment.2.Maxillary and mandibular premolars with single root and single canal.3.Patients with single rooted permanent teeth with periapical

radiolucency less than 1.5 mm as determined by an intraoral periapical (IOPA) radiograph.

4.Teeth with fully developed apex and straight canals with minimal curvature (0 to 10 degrees)

5.Teeth with healthy periodontium with periodontal probing depth

Exclusion Criteria

1.Pregnant women and lactating mothers.

2. Patients with acute dentoalveolar abscess or cellulitis.

3. Patients presenting with severe pain (75-100mm).

4. Patients who have taken antibiotics and analgesics and corticosteroid in the past month. 5.Patients with known immunocompromised conditions (e.g., AIDS)

6.Patients who are known diabetic.

7.Patients with non-vital teeth and intraoral and extraoral sinus tract

8.Patients with radiographic evidence of radiolucency of more than 1.5 mm

9. Patients who are having teeth with Single roots having multiple canals, bifurcation and trifurcation of canals, canal aberration, calcified canals. open apex, root resorption. presence of root caries and multirooted teeth

10. Teeth with aggressive periodontitis and grade III mobility, periodontal probing depth >3mm.

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
compare the of post-operative pain in <br/ ><br>single-visit endodontics where canal instrumentation will be done using <br/ ><br>two different rotary instrument systems. For each patient, the <br/ ><br>preoperative and post-operative pain levels will be recorded by using a <br/ ><br>visual analogue scale (VAS)Timepoint: The assessment of the post-operative pain will be conducted at intervals of 6 hours, 24 hours, and 7 days after the initial visit.

Secondary Outcome Measures