Clinical Trials Directory

Trials / Completed

CompletedNCT05530954

Direct Pulp Capping in Primary Molars

Clinical Evaluation of Direct Pulp Capping in Primary Molars

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
52 (actual)
Sponsor
Mansoura University · Academic / Other
Sex
All
Age
4 Years – 7 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to Assess the effect of MTA and hard setting Calcium Hydroxide (Dycal) on the clinical and radiographic outcome of direct pulp capping in primary molars and evaluate overall success rate of direct pulp capping in primary molars.

Detailed description

After informed consent, baseline clinical and radiographic assessment will be obtained and recorded in patient examination sheet. Participants who met the inclusion criteria were randomly allocated to two groups (n = 26/group, N = 52 in total) according to the capping martials using the envelope randomization method. 2 study groups according to capping material that will be used (Dycal or MTA) and each group will be divided to 2 subgroups according to site of exposure axial or pulpal. All patients were recalled and their treated molars were evaluated clinically and radiographically at 3months, 6months, 9months ,12months follow up periods.

Conditions

Interventions

TypeNameDescription
OTHERMineral trioxide aggregate (MTA)Materials for Vital Pulp Capping
OTHERHard setting Calcium Hydroxide (Dycal)Materials for Vital Pulp Capping

Timeline

Start date
2022-01-01
Primary completion
2023-05-27
Completion
2023-06-06
First posted
2022-09-07
Last updated
2023-09-26

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05530954. Inclusion in this directory is not an endorsement.