Sodiumhexametaphosphate Versus MTA as Pulp Capping Material for Immature Permanent Teeth

December 13, 2023 updated by: Mahmoud Ahmed Mahmoud, Minia University

Sodiumhexametaphosphate Versus MTA as Pulp Capping Material for Immature Permanent Teeth ( Randomized Clinical Trial)

Sodiumhexametaphosphate will be used as capping material for dental pulp of immature permanent teeth

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Estimated)

100

Phase

  • Not Applicable

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • healthy children
  • cooperative children
  • deep carious lesion
  • traumatic pulp exposure
  • immature permanent teeth

Exclusion Criteria:

  • uncooperative children
  • children with systemic disorders
  • non vital immature permanent teeth

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: MTA
Other: MTA
MTA
Other: Pulp capping
Pulp capping material for immature permanent teeth in case of carious or traumatic pulp expures
Experimental: Sodiumhexametaphosphate
Drug: Sodiumhexametaphosphate
Sodiumhexametaphosphate
Other: Pulp capping
Pulp capping material for immature permanent teeth in case of carious or traumatic pulp expures

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Clinical success
Time Frame: One year
Absence of pain, tenderness, mobility and swelling
One year
Radiographic success
Time Frame: One year
Absence of periapical lesions, internal resorption an external resorption also evidence of continuous root growth
One year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Minia University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

December 20, 2023

Primary Completion (Estimated)

December 20, 2024

Study Completion (Estimated)

January 20, 2025

Study Registration Dates

First Submitted

December 6, 2023

First Submitted That Met QC Criteria

December 13, 2023

First Posted (Estimated)

December 14, 2023

Study Record Updates

Last Update Posted (Estimated)

December 14, 2023

Last Update Submitted That Met QC Criteria

December 13, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 800

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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