Comparison of Sucess of Pulpotomy, Direct Pulp Capping and Indirect Pulp Capping Modalities Using MTA in Primary Teeth

NCT ID: NCT05020223

Last Updated: 2021-08-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

450 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-08-01

Study Completion Date

2023-09-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

450 healthy children with primary teeth of deep carious lesions without signs or symptomes of irreverisible pulp damage was selected randompy divoded into 3 groups each of 150 children that inder go vital pulp therapy through pulpotomy,direct pulp capping or indirect pulp capping using MTA as capping material for each modality then followed up for 2 years or more

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Deep Caries

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

MTA pulpotomy

Usuing MTA as capping material for cervical pulpotomy as a treatment option for deep carious primary teeth with signs and symptoms of reversible pulpitis in presence of pulp exposure

Group Type EXPERIMENTAL

Vital pulp therapy

Intervention Type OTHER

Vital pulp therapy different modalities for management of deep carious lesion in primary teeth

MTA direct pulp capping

Using MTA as capping material in case of trearment of deep carious primary teeth with signs and symptoms of reversible pulpitis with presence of pulp exposure

Group Type EXPERIMENTAL

Vital pulp therapy

Intervention Type OTHER

Vital pulp therapy different modalities for management of deep carious lesion in primary teeth

MTA indirect pulp capping

Using MTA as indirect capping material for treatment of deep carious primary teeth with signs and symptoms of reversible pulpitis

Group Type EXPERIMENTAL

Vital pulp therapy

Intervention Type OTHER

Vital pulp therapy different modalities for management of deep carious lesion in primary teeth

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Vital pulp therapy

Vital pulp therapy different modalities for management of deep carious lesion in primary teeth

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Healthy children
* Aged from 3 to 10 years old
* Deep cariuos primary tooth

Exclusion Criteria

* Primary teeth with any signs or syptoms of irreversible pulpitis
* Primary teeth of any signs or symptomes of vitality loss
* Primary teeth near to exfoliation
Minimum Eligible Age

3 Years

Maximum Eligible Age

10 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Minia University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Mahmoud Ahmed Mahmoud

Lecturer

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Minia University

Minya, , Egypt

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Egypt

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Mahmoud A Mahmoud

Role: CONTACT

01009578837

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Ahmad Elheeny, PhD

Role: primary

00201005560337

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

601

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.