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NCT04818658 Clinical Trial

The Preformed Metal Crowns Placed Using the Hall Technique Versus the Conventional Restoration

Dental Caries Clinical Trial

Official title:
The Preformed Metal Crowns Placed Using the Hall Technique Versus the Conventional Restoration: A 5-year Retro-prospective Clinical Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04818658
Other study ID # 441555555
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 8, 2021
Est. completion date December 10, 2021

Study information
Verified date July 2022
Source Bahçesehir University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to compare the survival rate of the conventional restorations with the Hall Technique in carious primary molars.

Description:

comparing the survival rate of the conventional restorations with the Hall Technique in carious primary molars.

Recruitment information / eligibility
Status Completed
Enrollment 26
Est. completion date December 10, 2021
Est. primary completion date October 3, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 5 Years to 8 Years
Eligibility Inclusion Criteria: - patients aged five to eight years at the time of dental treatment, - patients attending follow-up appointments - patients with compomer restoration and Hall restoration in their teeth - patients with matching the extent of caries in the two groups Exclusion Criteria: - patients not attending follow-up appointments - patients without both treatment

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Assessment of the stainless steel crown using the Hall Technique and Compomer Restoration on primary molars
Intra-oral clinical examination is performed and restorations are evaluated by the practitioner. Periapical radiography is taken according to national guidelines.

Locations
Country Name City State
Turkey Bahcesehir University Istanbul

Sponsors (1)
Lead Sponsor Collaborator
Bahçesehir University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary The survival rate of Hall Technique and Compomer Restorations Successful: restoration satisfactory, no additional treatment required, no clinical sign and symptoms of pulpal pathology or tooth exfoliated,
Minor failure: restoration wear/fracture/loss (restorable) or crown perforation, secondary caries or new caries, reversible pulpitis treated without requiring extraction or pulpotomy,
Major failure: the tooth is broken down (unrestorable), inter-radicular radiolucency or internal root resorption, signs or symptoms of irreversible pulpitis requiring extraction or pulpotomy.
The survival analysis: the restorations are assessed as successful or failure.		 5 year
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