- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07622719
Survey on Knowledge and Acceptance of Dental General Anesthesia for Children Among Different Populations
June 1, 2026 updated by: Zhang Baize, Air Force Military Medical University, China
A Survey on the Cognition and Acceptance of Pediatric Dental General Anesthesia Techniques
This is a cross-sectional, questionnaire-based study conducted in China.
The purpose of this study was to investigate the knowledge and acceptance of pediatric dental general anesthesia among different populations, including parents, dental professionals, and the general public.
Participants completed an anonymous online questionnaire assessing their understanding of the procedure, perceived risks and benefits, and willingness to accept dental general anesthesia for children.
No medical interventions were provided to participants.
The findings aim to provide evidence for improving patient education and promoting informed decision-making regarding pediatric dental treatment under general anesthesia
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This is a cross-sectional questionnaire-based survey.
Study Type
Observational
Enrollment (Actual)
1490
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Shanxi
-
Xi’an, Shanxi, China, 710032
- School of Stomatology, The Fourth Military Medical University,Xi'an, Shaanxi 710032
-
Xi’an, Shanxi, China, 710032
- Yaping Shi
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
The study population consists of parents of children receiving dental treatment, dental healthcare professionals, and the general public aged 20 years and older.
Participants were recruited from hospital settings and online platforms to complete a questionnaire-based survey on knowledge and acceptance of pediatric dental general anesthesia.
Description
Inclusion Criteria:
- Aged ≥20 years
- Able to understand and complete the questionnaire
- Informed consent obtained
Exclusion Criteria:
- Cognitive impairment or inability to communicate
- Refusal to participate -
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
All Participants
All participants completed the questionnaire survey on knowledge and acceptance of pediatric dental general anesthesia.
|
A self-administered questionnaire assessing knowledge and acceptance of pediatric dental general anesthesia, no active intervention provided.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Acceptance Score of Pediatric Dental General Anesthesia
Time Frame: "baseline, pre-intervention"
|
Acceptance level of pediatric dental general anesthesia techniques (measured by "A Survey on the Cognition and Acceptance of Pediatric Dental General Anesthesia Techniques", ranging from 1 (lowest acceptance) to 5 (highest acceptance), where higher scores indicate a better outcome).
|
"baseline, pre-intervention"
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Correlation between Demographic Factors and Acceptance
Time Frame: "baseline, pre-intervention"
|
Correlation between demographic factors (age, education level, and occupation) and acceptance of pediatric dental general anesthesia, assessed at the time of survey completion.
|
"baseline, pre-intervention"
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 1, 2026
Primary Completion (Actual)
April 30, 2026
Study Completion (Actual)
April 30, 2026
Study Registration Dates
First Submitted
May 21, 2026
First Submitted That Met QC Criteria
June 1, 2026
First Posted (Actual)
June 3, 2026
Study Record Updates
Last Update Posted (Actual)
June 3, 2026
Last Update Submitted That Met QC Criteria
June 1, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- KQ-2026-Q-010
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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