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Clinical and Radiographic Evaluation in Pulpotomy of Primary Molars Using Protooth Vs. MTA

NCT04710160 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2021-08-05

No results posted yet for this study

Summary

The aim of the study is to evaluate the clinical and radiographic success in pulpotomy using novel fast-setting calcium silicate cement (Protooth) versus MTA in exposed primary molars.

Conditions

  • Clinical Evaluation Including Pain and Swelling

Interventions

DRUG

Novel fast-setting calcium silicate cement (Protooth)

In form of power and liquid to be mixed together to form a paste.

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
4 Years
Max Age
8 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-08-31
Primary Completion
2022-10-22
Completion
2022-11-30

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04710160 on ClinicalTrials.gov