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Clinical Success of Anterior and Posterior Crowns in a Group of Children Treated Under General Anesthesia

Not yet recruiting
Conditions
Prosthesis Failure, Dental
Registration Number
NCT06201481
Lead Sponsor
Cairo University
Brief Summary

* This incidence study aims to evaluate the clinical success of anterior and posterior full-coverage restorations among a group of Egyptian children treated under general anesthesia.

* The main question it aims to answer:

In A Group of Children, What Is the Clinical Success of Anterior and Posterior Full Coverage Restorations Performed Under General Anesthesia?

Detailed Description

This study consisted of clinical examinations of the participants treated under general anesthesia to evaluate the clinical success of anterior and posterior crowns that will be performed on the day of the dental treatment, then after 15 days, 3, 6, and 12 months recall examinations.

- The level of parental satisfaction will be evaluated through a questionnaire that will be completed after 15 days, 3, 6, and 12 months.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
100
Inclusion Criteria
  • Children aged between 2 and 5 years old.
  • Children classified as American Society of Anesthesiologists class I; Healthy (no acute or chronic disease, normal BMI percentile for age)
  • All Children received pulp therapy techniques for vital teeth.
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Exclusion Criteria
  • Children with mental or neurological disorders.
  • Children with developmental disorders and syndromes.
  • Children whose parents have no mobile phone access.
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Clinical Success of Stainless-Steel CrownsImmediately after the intervention then after 15 days then after 3 months then after 6 months and after 12 months

Clinical evaluation criteria:

* crown marginal adaptation

* crown marginal extension crown proximal contact

* duration of crown presence

Clinical Success of Anterior Esthetic CrownsImmediately after the intervention then after 15 days then after 3 months then after 6 months and after 12 months

Clinical evaluation criteria:

* crown retention

* crown chipping

* opposing wear

Secondary Outcome Measures
NameTimeMethod
Pain scoreImmediately after the intervention then after 15 days then after 3 months then after 6 months and after 12 months

Pain will be evaluated by scores using a five-point scale.

* None (If the parents give a score 1)

* Mild (If the parents give a score 2)

* Moderate (If the parents give a score 3)

* Sever (If the parents give a score 4 or 5)

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