Clinical effectiveness of newer pulpotomy agents

Not Applicable

Conditions: Health Condition 1: K040- Pulpitis

Registration Number: CTRI/2022/04/042044

Lead Sponsor: S B Divya

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: ot Yet Recruiting

Sex: Not specified

Target Recruitment: 0

Inclusion Criteria

1)Patients with symptomatic Irreversible Pulpitis of age 18 to 40 years permanent mature molar teeth with symptomatic irreversible pulpitis

2)Both Maxillary and Mandibular molar teeth.

3) A clinical diagnosis consistent with irreversible pulpitis will be established in all cases based on a history of severe spontaneous lingering pain that could be reproduced by cold testing.

4)Teeth which are tender to percussion can be included but those with periapical lesions, resorption of root must be excluded.

Exclusion Criteria

1)Patients < 18years of age.

2)Patients of age > 40 years of age

3)Medically compromised patients

4)Pregnant and lactating women.

5)Patients undergoing fixed orthodontic therapy

6)Patients with facial deformity including cleft lip/palate.

7)Teeth with apical periodontitis.

8)Teeth with fracture or crack lines.

9)Teeth with abrasion on the same tooth.

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Post operative pain , tenderness and swelling (yes or no) <br/ ><br>Pain will be assessed using Visual Analog Scale (VAS) <br/ ><br>Timepoint: Post operative pain will be assessed after 24 hours and 48 hours, tenderness and swelling (yes or no)will be checked after 48 hours and 3 months <br/ ><br>Pain will be assessed using Visual Analog Scale (VAS) <br/ ><br>

Secondary Outcome Measures

Name	Time	Method
Presence of periapical lesions at 3, 6 & 12 months recall. Dentin bridge formation at 12 months interval through CBCT radiographic analysis. <br/ ><br>Timepoint: 3,6,12 months