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

Clinical Success of Anterior and Posterior Full Coverage Restorations in a Group of Children Treated Under General Anesthesia: An Incidence Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06201481
Enrollment
100
Registered
2024-01-11
Start date
2024-08-01
Completion date
2025-10-31
Last updated
2024-06-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prosthesis Failure, Dental

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.

Interventions

PROCEDUREanterior and posterior full coverage crowns

Teeth preparation,crown fitting and cementation

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
2 Years to 5 Years
Healthy volunteers
Yes

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.

Exclusion criteria

* Children with mental or neurological disorders. * Children with developmental disorders and syndromes. * Children whose parents have no mobile phone access.

Design outcomes

Primary

MeasureTime frameDescription
Clinical Success of Stainless-Steel CrownsImmediately after the intervention then after 15 days then after 3 months then after 6 months and after 12 monthsClinical 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 monthsClinical evaluation criteria: * crown retention * crown chipping * opposing wear

Secondary

MeasureTime frameDescription
Pain scoreImmediately after the intervention then after 15 days then after 3 months then after 6 months and after 12 monthsPain 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)

Other

MeasureTime frameDescription
Level of Parental SatisfactionAfter 15 days of the Intervention then after 3 months then after 6 months and after 12 monthsA 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?

Contacts

Primary ContactSalma Sayed, B.D.S
salmasayed25@gmail.com01066364181
Backup ContactHanaa Abdelmoniem, PhD
01001081614

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026