Comparision of Protooth Cement and Biodentine in Indirect Pulp capping in Children.

Phase 4

Conditions: Health Condition 1: K040- Pulpitis

Registration Number: CTRI/2024/05/067871

Lead Sponsor: Dr N Devi Vyshnavi

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: ot Yet Recruiting

Sex: Not specified

Target Recruitment: 0

Inclusion Criteria

Clinical:

1)The primary molars with no spontaneous pain, no tenderness to percussion or palpation

2)Primary molars with a deep carious lesion approximating pulp.

3)Presence of active carious lesions involving occlusal surfaces of primary molars.

4)Extension of carious lesion such that complete caries removal would risk pulp exposure.

5)Cooperative children and parents willing to follow the instructions and report for follow-up.

Radiographic:

1)No radiographic signs of internal or external root resorption

2)Radiographic evidence of an intact lamina dura.

3)Dental caries close to the pulp.

Exclusion Criteria

Clinical:

1)Patients who decline to participate in the study.

2)History of spontaneous sharp, penetrating pain, or tenderness on percussion.

3)Presence of abnormal tooth mobility, fistula, abscess, and swelling of the soft and periodontal tissues.

4)Presence of chronic systemic diseases.

Radiographic:

1)Large carious lesion with radiographic pulp exposure.

2)Presence of interrupted lamina dura, internal or external root resorption, interradicular or periapical pathosis, and widened periodontal ligament space

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To compare the clinical & radiographic success rate of indirect pulp capping in primary molars using protooth and biodentine.Timepoint: Baseline, 1 month, 3 months , 6 months <br/ ><br>

Secondary Outcome Measures