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NOT YET RECRUITING
NCT06468085
NA

Evaluation of Pulpotomy Using Two Different Agents in Mature Anterior Teeth With Pulpitis

Sponsor: Ain Shams University

View on ClinicalTrials.gov

Summary

the study will evaluate the clinical and radiological success of mature permanent anterior teeth pulpotomy in children and adolescents with signs of pulpitis using two different Biomimetic materials (NeoPutty® and Biodentine™) as a pulp dressing material in comparison to root canal treatment at 3, 6, 9 and 12 months follow up.

Official title: Clinical and Radiographic Evaluation of Premixed Bioceramic Putty and Biodentine™ Pulpotomy in Mature Permanent Anterior Teeth With Signs of Pulpitis: A Randomized Controlled Trial

Key Details

Gender

All

Age Range

9 Years - 14 Years

Study Type

INTERVENTIONAL

Enrollment

48

Start Date

2024-07-01

Completion Date

2026-07-01

Last Updated

2024-06-21

Healthy Volunteers

Yes

Conditions

Interventions

PROCEDURE

premixed Bioceramic NeoPUTTY®

Pulpotomy procedure will be performed after hemostasis followed by covering pulp stump with Premixed Bioceramic then final composite restoration will be applied. clinical evaluation will be done at baseline, 3, 6, 9 and 12 months.

PROCEDURE

Biodentine™

Pulpotomy procedure will be performed after hemostasis followed by covering pulp stump with Premixed Bioceramic or Biodentine™ according to the corresponding group then final composite restoration will be applied. clinical evaluation will be done at baseline, 3, 6, 9 and 12 months.

PROCEDURE

Root canal treatment

Root canal treatment will be performed to the control group followed by composite restoration. clinical evaluation will be done at baseline, 3, 6, 9 and 12 months.