Endocrown Restoring First Permanent Molar in Children

NCT ID: NCT06432049

Last Updated: 2024-05-29

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

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-12-05

Study Completion Date

2024-05-13

Brief Summary

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

Clinical and radiographic evaluation of endodontically treated first permanent molars in thirty children restored with three different restorations over 12 months

Detailed Description

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

This study comprised 30 children, with age range of (10-13) years old, with endodontically treated first permanent molars. Participants were classified into three groups according to type and material of the final restoration. All selected children were assigned to either PMC group (n=10) restored with performed metal crowns (Stainless-steel Molar Crowns) , EMX group (n=10) endocrown fabricated from CAD-CAM lithium disilicate glass ceramic , COP group (n=10) endocrown fabricated from CAD-CAM reinforced composite. After cementation, all children were evaluated over one year; at one week post-operative, 6 and 12 months for the following criteria: radiographic findings, plaque index, periodontal index, parent satisfaction.

Conditions

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

Comparing Different Types of Restorations for Restoring Endodontically Treated Permanent First Molar in Children

Study Design

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

Allocation Method

RANDOMIZED

Intervention Model

FACTORIAL

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.

PMC

endodontically treated molar restored with Stainless steel crown

Group Type EXPERIMENTAL

restoration for endodontically treated molar

Intervention Type OTHER

prefabricated stainless steel crown or endocrown

EMX

endodontically treated molar restored with endocrown fabricated from CAD-CAM lithium disillicate

Group Type EXPERIMENTAL

restoration for endodontically treated molar

Intervention Type OTHER

prefabricated stainless steel crown or endocrown

COP

endodontically treated molar restored with endocrown fabricated from CAD-CAM composite

Group Type EXPERIMENTAL

restoration for endodontically treated molar

Intervention Type OTHER

prefabricated stainless steel crown or endocrown

Interventions

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

restoration for endodontically treated molar

prefabricated stainless steel crown or endocrown

Intervention Type OTHER

Eligibility Criteria

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

Inclusion Criteria

* Patient age ranging from 10-13 years old with closed apex.
* Normal occlusion without any para-functional habits.
* Decayed lower first molar.
* Supra-gingival margin was required after preparation.
* Absence of root fractures or cracks.

Exclusion Criteria

* Difficulty to apply rubber dam for proper endocrown bonding.
* Lack of patient cooperation for post-operative recall and follow up.
* Bad oral hygiene
Minimum Eligible Age

10 Years

Maximum Eligible Age

13 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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

Kafrelsheikh University

OTHER

Sponsor Role lead

Responsible Party

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

Ahmed Ismail Taha

lecturer

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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

Kafr El Shaikh University

Kafr ash Shaykh, , Egypt

Site Status

Countries

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

Egypt

References

Explore related publications, articles, or registry entries linked to this study.

Taha AI, Saad AE. Clinical and radiographic outcomes of endocrowns fabricated from two different CAD-CAM materials versus stainless steel crowns in restoring first permanent molars in children: a randomized clinical trial. BMC Oral Health. 2025 Jul 8;25(1):1127. doi: 10.1186/s12903-025-06507-z.

Reference Type DERIVED
PMID: 40629344 (View on PubMed)

Other Identifiers

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

MKSU/22-11-4

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

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

Aesthetic Restorations in Deciduous Anterior Teeth
NCT05875064 NOT_YET_RECRUITING PHASE3