Clinical and Radiographic Evaluation of Resin Endocrown as Long Term Interim Restoration Versus Stainless Steel Crown for Endodontically Treated First Permanent Molar in Children: Randomized Controlled Pilot Study.

NCT ID: NCT05250609

Last Updated: 2023-10-03

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

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

24 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-08-01

Study Completion Date

2023-09-30

Brief Summary

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management of endodontically treated first permanent molar with deep dental caries is one of the challenging procedure that the operator face. Using resin endocrown or stainless steel crown restoration to make comparison which one is more successful in children.

Detailed Description

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Diagnostic procedure:

Diagnosis of the cases will be performed according to guidelines of AAPD 2017 for treatment of irreversible pulpitis and necrotic pulp therapy in mandibular first permanent molar . Preoperative periapical radiograph will be taken

Intra operative procedure:

Local anaesthesia administration using articaine 4% with epinephrine 1:100000. Rubber dam application and access cavity preparation will be established using a sterile bur. Root Canal Treatment will be done and then the dental orifices of the pulp chamber will be sealed using a flowable composite.

The immediate postoperative radiograph will be done to reveal optimal root canal treatment.

In the intervention group:

The preparation of cavity design will be as following:

Preparation of occlusal surface will be done with wheel stone to create 2 mm occlusal clearance; the occlusal surface will be prepared flat to create a butt-joint. The junction between the occlusal and mesial cavity will be rounded to produce cervical side walk. • Divergence of the inner cavity walls will be obtained using a tapered stone with a rounded end (TR- Dia Bur Mani).

Impression will be taken for the prepared tooth structure using addition silicone material (Elite HD Zermach, Italy), stone model will be poured for fabrication of endocrown to allow for blockage of any undercuts in the pulp chamber cavity. Finished final endocrown restoration will be cemented in place using self-adhesive universal dual cured resin cement (rely X Unicem, 3M, USA).

In the control group tooth preparation will be made as follow:

By reducing mesial, distal and occlusal surface. The crown margin will be placed just apically to the gingival margin and carefully adjusted to give an accurate fit in this region. The crown will be cemented with glass ionomer cement.

Follow up:

Clinical and evaluation will be performed at 1 st week, 3, 6, 9 and 12 months. Radiograph evaluation will be performed at, 1 st week, 6 and 12 months

Conditions

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Dental Caries in Children

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Caregivers Outcome Assessors
The statistician will be blinded throughout the whole procedures (double blind). Principle investigator will be responsible for all clinical procedures.

Study Groups

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Intervention: Endocrown "composite".

Composite Endocrown will be used as an extra-coronal restoration in endodontically treated mutilated first permanent molar

Group Type EXPERIMENTAL

Endocrown "composite".

Intervention Type OTHER

It is a type of restoration has been shown a great success in adult and recently has been suggested for children

Comparator / Control: Stainless steel crown.

Stainless steel crown will be used as an extra-coronal restoration in endodontically treated mutilated first permanent molar

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Endocrown "composite".

It is a type of restoration has been shown a great success in adult and recently has been suggested for children

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Cooperative children in age range from 10 to 13 years

* Mandibular first permanent molar indicated for root canal treatment with closed apex.
* Presence of at least two to three sound walls of tooth.
* Absence of internal or external pathologic root resorption.
* Normal occlusion without any para-functional habits.
* Parent or guardian agree for participant in the study

Exclusion Criteria

* Excessive mobility.
* Children with underlying systemic disease.
* Children with special health care needs.
* Poor oral hygiene.
Minimum Eligible Age

10 Years

Maximum Eligible Age

13 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Cairo University

OTHER

Sponsor Role lead

Responsible Party

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Basheer Ali Mabkhot

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Basheer MAbkhot

Cairo, Jiza, Egypt

Site Status

Countries

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Egypt

References

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Mabkhot BA, Taha SEE, Sabry SM. Clinical and radiographic assessment of composite CAD/CAM endocrowns and stainless steel crowns for endodontically treated first permanent molars in Egyptian children: randomized controlled pilot study. BMC Oral Health. 2025 May 31;25(1):864. doi: 10.1186/s12903-025-06192-y.

Reference Type DERIVED
PMID: 40450229 (View on PubMed)

Other Identifiers

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14422021510951

Identifier Type: -

Identifier Source: org_study_id

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