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
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Basic Information
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COMPLETED
NA
24 participants
INTERVENTIONAL
2022-08-01
2023-09-30
Brief Summary
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Detailed Description
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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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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
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
Endocrown "composite".
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
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
Eligibility Criteria
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Inclusion Criteria
* 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
* Children with underlying systemic disease.
* Children with special health care needs.
* Poor oral hygiene.
10 Years
13 Years
ALL
No
Sponsors
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Cairo University
OTHER
Responsible Party
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Basheer Ali Mabkhot
Principal Investigator
Locations
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Basheer MAbkhot
Cairo, Jiza, Egypt
Countries
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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.
Other Identifiers
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14422021510951
Identifier Type: -
Identifier Source: org_study_id
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