Biological properties of white mineral trioxide aggregate mixed with sodium hypochlorite gel

Not Applicable

Completed

• Conditions: Oral Health; Dental caries

• Registration Number: ISRCTN58885533
• Lead Sponsor: Damascus University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2024-06-02
• Study Start: 2024-07-03
• Last Update Posted: 15 July 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 24

Inclusion Criteria

1. Children aged 8-10 years
2. Children with at least 2 bilateral carious first primary molars indicated for pulpotomy
3. Children require serial extraction of first primary molars for orthodontic reasons

Exclusion Criteria

1. Children with systematic diseases and/or allergies to the anesthetic agents
2. Children with clinical and radiographical signs of pulp necrosis in the targeted teeth and/or unrestorable teeth
3. Children with nocturnal and/or spontaneous pain

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The following primary outcomes will be measured using histology after 7, 30, and 90 days:<br>1. Odontoblastic integrity<br>2. Pulp tissue hemorrhage<br>3. Pulp fibrosis<br>4. Dentin bridge formation<br>5. Pulp calcification

Secondary Outcome Measures

Name	Time	Method
There are no secondary outcome measures