Comparative Study Between Biodentine and Mineral Trioxide Aggregate in Direct Pulp Capping

Not Applicable

Completed

• Conditions: Patients With Deep Carious Lesions
• Interventions: Drug: Biodentine; Drug: MTA

• Registration Number: NCT02803528
• Lead Sponsor: Damascus University

Brief Summary

Comparative study between Biodentine and MTA in direct pulp capping of deeply carious teeth.

Detailed Description

Not available

Study Timeline

• Study Start: 2015-01
• Study First Submitted: 2016-06-14
• Study First Submitted QC: 2016-06-14
• Study First Posted: 2016-06-17
• Primary Completion: 2017-01-20
• Study Completion: 2017-10-20
• Status Verified: 2017-12
• Last Update Submitted: 2017-12-31
• Last Update Posted: 2018-01-03

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

1. asymptomatic vital molars (upper or lower)
2. with complete formation of roots
3. Aged 15 to 30 years.
4. Accidental point pulp exposure during the process of removing dental caries.

Exclusion Criteria

1. If the molar not vital.
2. If the molar is symptomatic.
3. Immature molar.
4. Patient not in age between (15-30 years).

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Biodentine	Biodentine	The exposed area of the pulp is going to be covered with Biodentine.
MTA	MTA	The exposed area of the pulp is going to be covered with MTA

Primary Outcome Measures

Name	Time	Method
Success at 3 months following capping	the success of treatment is assessed at three months following the application of the material	Case is considered successful if clinical and radiographic examinations of tooth are sound 100%.
Success at 6 months following capping	the success of treatment is assessed at six months following the application of the material	Case is considered successful if clinical and radiographic examinations of tooth are sound 100%.
Success at 18 months following capping	the success of treatment is assessed at 18 months following the application of the material	Case is considered successful if clinical and radiographic examinations of tooth are sound 100%.
Success at 24 months following capping	the success of treatment is assessed at 24 months following the application of the material	Case is considered successful if clinical and radiographic examinations of tooth are sound 100%.
Success at 9 months following capping	the success of treatment is assessed at 9 months following the application of the material	Case is considered successful if clinical and radiographic examinations of tooth are sound 100%.
Success at 12 months following capping	the success of treatment is assessed at 12 months following the application of the material	Case is considered successful if clinical and radiographic examinations of tooth are sound 100%.

Trial Locations

Locations (1)

Department of Operative Dentistry, University of Damascus Dental School; 🇸🇾 Damascus, Syrian Arab Republic