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Custom-made Versus Prefabricated Zirconia Crowns for Primary Molars.

Primary Purpose

Decayed Teeth

Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Custom-made zirconia crowns
Prefabricated zirconia crowns
Sponsored by
Al-Azhar University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Decayed Teeth focused on measuring Zirconia Crown, Primary teeth

Eligibility Criteria

5 Years - 9 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Children of 5-9 years old.
  2. The children have at least 2 decayed primary molars.
  3. Presence of an intact contralateral primary molar as a control.
  4. Willingness to participate and to continue with the follow up appointments.
  5. Clinical and radiographically confirmed dental caries extending to the middle third of dentin.
  6. Presence of teeth in opposite arch with normal occlusion.

Exclusion Criteria:

  1. Children with systemic health problem.
  2. Children with periodontal disease.
  3. Children with unilateral chewing habit or allergic to local anesthesia.
  4. Presence of parafunctional habit.

Sites / Locations

  • Roqaia M Alassar

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Custom-made zirconia crowns Group

Prefabricated zirconia crowns Group

Arm Description

Ten decayed primary molars will be restored with custom-made zirconia crowns.

Ten decayed primary molars will be restored with prefabricated zirconia crowns.

Outcomes

Primary Outcome Measures

Change in periodontal health.
The periodontal health will be assessed using the plaque index (PI) and the gingival index (GI)

Secondary Outcome Measures

Change in clinical performance.
The clinical success of the crowns will be assessed in terms of crown retention, marginal adaptation, crown contour, fracture, stain resistance, opposing tooth wear and tooth exfoliation.

Full Information

First Posted
November 3, 2020
Last Updated
September 3, 2023
Sponsor
Al-Azhar University
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1. Study Identification

Unique Protocol Identification Number
NCT04620174
Brief Title
Custom-made Versus Prefabricated Zirconia Crowns for Primary Molars.
Official Title
Custom-made Versus Prefabricated Zirconia Crowns for Primary Molars; a Clinical Trial With 12-month Follow-up.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Completed
Study Start Date
December 1, 2020 (Actual)
Primary Completion Date
July 1, 2022 (Actual)
Study Completion Date
July 1, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Al-Azhar University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Background: Do construction methods of pediatric zirconia crowns affect the periodontal health and clinical performance of badly decayed primary molars? The question asked by many practitioners. Purpose: to compare the periodontal health and clinical performance of primary molars restored with custom-made and prefabricated zirconia crowns. Hypothesis is the performance of primary molars restored with custom-made zirconia crowns will be equivalent to those restored with prefabricated zirconia crowns.
Detailed Description
This study is a randomized, 12-month follow up clinical trial. According to sample size calculation, ten patients will be selected in conjunction with departments of Pedodontics and Crowns & Bridges. The study will be conducted in accordance with the principles of the Research Ethics Committee, Faculty of Dental Medicine for Girls, Al-Azhar University, Egypt. The purpose of the investigation and the clinical procedures of this study will be explained to the parents and children. A written informed consent form will be signed from patient guardians and obtained prior to study initiation. The inclusion and exclusion criteria are established as the following; Inclusion criteria Children of 5-9 years old. The children have at least 2 pulpotomized primary molars with no clinical signs & symptoms or periapical pathosis. Presence of an intact contralateral primary molar as a control. Willingness to participate and to continue with the follow up appointments. Clinical and radiographically confirmed dental caries extending to the middle third of dentin. Presence of teeth in opposite arch with normal occlusion. Exclusion criteria Children with systemic health problem. Children with periodontal disease. Children with unilateral chewing habit or allergic to local anesthesia. Presence of parafunctional habit. Clinical procedure; Patient selection and education; The participating children will continue with their routine dental appointments in the undergraduate training clinic. Before beginning, children, along with their parents will receive a standard oral hygiene education by an undergraduate student through brushing demonstration on a model. Parents will be warned when signs of gingival inflammation are present, or plaque control is inadequate. Samples grouping and teeth preparation: Forty primary molars will be included in the study. Twenty decayed teeth will be restored with crowns (10 with custom-made ZrCs and 10 with prefabricated ZrCs), and the other twenty intact contralateral teeth will be evaluated as the controls (10 molars will be the controls for custom-made ZrCs and 10 molars will be the controls for prefabricated ZrCs). Preparation of the crowns will be performed under local anesthesia, according to manufacturers' instructions with the following guidelines; 1-2mm occlusal reduction, 0.5-1mm axial reduction, and a chamfer finish line will be established 0.5-1mm subgingivally. Impression taking and temporization: After preparation, rubber-base impressions will be taken for the teeth specific for custom-made ZrCs. Then SSCs will be temporarily cemented over the prepared teeth till the next appointment. Try-in and cementation of ZrCs: SSCs will be removed and the custom-made and prefabricated ZrCs will be tried in and permanently cemented. Follow-up visits: The participants will be recalled for evaluation after a baseline and at 1, 3, 6 and 12 months. • Evaluation methods: The periodontal health will be assessed using the plaque index (PI) and the gingival index (GI). The clinical success of the crowns will be assessed in terms of crown retention, marginal adaptation, crown contour, fracture, stain resistance, opposing tooth wear and tooth exfoliation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Decayed Teeth
Keywords
Zirconia Crown, Primary teeth

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Three groups will be included; Custom-made Zirconia Crowns Group (10 molars) Prefabricated Zirconia Crowns Group (10 molars)
Masking
Participant
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Custom-made zirconia crowns Group
Arm Type
Other
Arm Description
Ten decayed primary molars will be restored with custom-made zirconia crowns.
Arm Title
Prefabricated zirconia crowns Group
Arm Type
Other
Arm Description
Ten decayed primary molars will be restored with prefabricated zirconia crowns.
Intervention Type
Other
Intervention Name(s)
Custom-made zirconia crowns
Intervention Description
Ten decayed primary molars will be restored with custom-made zirconia crowns.
Intervention Type
Other
Intervention Name(s)
Prefabricated zirconia crowns
Intervention Description
Ten decayed primary molars will be restored with prefabricated zirconia crowns.
Primary Outcome Measure Information:
Title
Change in periodontal health.
Description
The periodontal health will be assessed using the plaque index (PI) and the gingival index (GI)
Time Frame
At 1, 3, 6 and 12 months following application.
Secondary Outcome Measure Information:
Title
Change in clinical performance.
Description
The clinical success of the crowns will be assessed in terms of crown retention, marginal adaptation, crown contour, fracture, stain resistance, opposing tooth wear and tooth exfoliation.
Time Frame
At 1, 3, 6 and 12 months following application.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
9 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children of 5-9 years old. The children have at least 2 decayed primary molars. Presence of an intact contralateral primary molar as a control. Willingness to participate and to continue with the follow up appointments. Clinical and radiographically confirmed dental caries extending to the middle third of dentin. Presence of teeth in opposite arch with normal occlusion. Exclusion Criteria: Children with systemic health problem. Children with periodontal disease. Children with unilateral chewing habit or allergic to local anesthesia. Presence of parafunctional habit.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Noha I Metwally, DDS
Organizational Affiliation
Pedodontist, Faculty of Dental Medicine for Girls, Al-Azhar University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Asmaa M Abdelgawad, DDS
Organizational Affiliation
Fixed Prosthodontist, Faculty of Dental Medicine for Girls, Al-Azhar University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Roqaia M Alassar, DDS
Organizational Affiliation
Fixed Prosthodontist, Faculty of Dental Medicine for Girls, Al-Azhar University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Roqaia M Alassar
City
Cairo
ZIP/Postal Code
11765
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
No

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Custom-made Versus Prefabricated Zirconia Crowns for Primary Molars.

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