Actively Recruiting
Sedation Versus Protective Stabilization for Pediatric Dental Treatment
Led by Universidade Federal de Goias · Updated on 2024-12-10
152
Participants Needed
2
Research Sites
317 weeks
Total Duration
On this page
Sponsors
U
Universidade Federal de Goias
Lead Sponsor
U
University of Sao Paulo
Collaborating Sponsor
AI-Summary
What this Trial Is About
There is a lack of evidence on the effectiveness of moderate sedation in pediatric dentistry, compared to protective stabilization, which remains routinely used in the Brazilian context despite moral questions. The objective of this prospective nonrandomized clinical trial is to evaluate the effectiveness of the use of moderate sedation, compared to the protective stabilization, in the dental care of children with fear / anxiety and / or dental behavior problem, and associated factors. The study will be carried out in outpatient clinics of the Dental Schools of the Federal University of Goiás (UFG) and University of São Paulo (USP), with the support of professors from King's College London through the partnership CEDACORE - Children Experiencing Dental Anxiety: Collaboration on Research and Education. Participants will be 152 children under 7 years of age with dental caries, who need specialized dental treatment due to a history of non-cooperation with dental care. The interventions to be compared are moderate sedation with oral administration of ketamine and midazolam (UFG) and protective stabilization (USP). The primary endpoint 'behavior / anxiety of the child during treatment will be assessed using the Ohio State University Behavioral Rating Scale. The secondary outcomes are: dental behavioral and anxiety evolution of the child, child' pain during procedure, impact on the quality of life related to oral health, parents and dentists' satisfaction and stress, adverse events for sedated participants, longevity of composite and glass ionomer cement restorations, chronotype and physiological stress of these children. A cost-efficacy analysis will be produced at the end of the study from the perspective of the Sistema Único de Saúde. Additionally, at the end of 36 months, the investigators expect to contribute to the identification of psychosocial aspects related to dental behavior problems in children in early childhood. It is important to highlight the perspective of technological innovation, with the creation of a digital platform that will allow the registration of data related to the dental care of children worldwide and favor analyzes in the methodology of data science.
CONDITIONS
Official Title
Sedation Versus Protective Stabilization for Pediatric Dental Treatment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Children presenting cavities that need dental restoration
- ASA I (healthy) or II (mild and controlled systemic disease, for example persistent asthma) children
- Medical history without neurological or cognitive impairment
- Children who do not use medicines that may impair cognitive functions
- Children at low risk for airway obstruction (Mallampati less than 2 and/or tonsil hypertrophy occupying less than 50% of the oropharynx)
You will not qualify if you...
- Children with positive or definitely positive behavior in the dental examination session
- Non-attendance at the first intervention appointment after three scheduling attempts
- Chronic use of systemic corticosteroids
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Dental School - UFG
Goiânia, Goiás, Brazil, 74605220
Active, Not Recruiting
2
Dental School - FOUSP
São Paulo, São Paulo, Brazil, 05508-000
Actively Recruiting
Research Team
P
Patricia C Faria, PhD
CONTACT
L
Luciane R Costa, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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