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

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age2-5
SponsorCairo University

About this trial

* 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?

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

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.

Disqualifiers

Children with mental or neurological disorders.

Children with developmental disorders and syndromes.

Children whose parents have no mobile phone access.

Trial population

Egyptian Children Aged 2-5 years.

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • anterior and posterior full coverage crowns

    Procedure/Surgery

    Teeth preparation,crown fitting and cementation

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Clinical Success of Stainless-Steel Crowns

Clinical evaluation criteria: * crown marginal adaptation * crown marginal extension crown proximal contact * duration of crown presence

Time frame
Immediately after the intervention then after 15 days then after 3 months then after 6 months and after 12 months
2

Clinical Success of Anterior Esthetic Crowns

Clinical evaluation criteria: * crown retention * crown chipping * opposing wear

Time frame
Immediately after the intervention then after 15 days then after 3 months then after 6 months and after 12 months

Secondary outcomes

1

Pain score

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)

Time frame
Immediately after the intervention then after 15 days then after 3 months then after 6 months and after 12 months

Other outcomes

1

Level of Parental Satisfaction

A questionnaire will measure the level of parental satisfaction. \- Questions will be answered by YES or NO . The questions : * Received enough information before treatment? * Knew where and how to access help after treatment? * Regarded this treatment to be positive? * Overall experience is satisfactory? * Would consider general anesthesia for treatment again?

Time frame
After 15 days of the Intervention then after 3 months then after 6 months and after 12 months

Locations

This trial has no locations.

Sponsors and contacts

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