Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06922578

Clinical and Radiographic Success of Pulpotomy Using Neoputty Mineral Trioxide Aggregate Versus Pulpectomy Using Endoflas In Primary Molars With Irreversible Pulpitis: A Randomized Controlled Trial

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
66 (estimated)
Sponsor
Cairo University · Academic / Other
Sex
All
Age
4 Years – 9 Years
Healthy volunteers
Accepted

Summary

The goal of this randomized clinical trial is to evaluate the clinical and radiographic success of pulpotomy using Neoputty MTA vital primary molars diagnosed with symptomatic irreversible pulpitis. The main question it aims to answer is: Will Neoputty MTA pulpotomy have higher clinical and radiographic success in comparison to Endoflas pulpectomy in primary molars with irreversible pulpitis?

Conditions

Interventions

TypeNameDescription
PROCEDURENeoPUTTY MTA pulpotomyNeoputty MTA pulpotomy performed in vital primary molars with symptomatic irreversible pulpitis
PROCEDUREEndoflas pulpectomyEndoflas pulpectomy in vital primary molars with symptomatic irreversible pulpitis

Timeline

Start date
2025-05-01
Primary completion
2026-05-01
Completion
2026-06-01
First posted
2025-04-10
Last updated
2025-04-10

Source: ClinicalTrials.gov record NCT06922578. Inclusion in this directory is not an endorsement.