Survey on Patient and Parental Perceptions of EEG-monitoring During Paediatric Anaesthesia Care
April 22, 2025 updated by: KK Women's and Children's Hospital
Electroencephalographic (EEG) monitoring during general anaesthesia (GA) is not typically part of standard care during GA.
The recent availability of non-invasive commercial EEG monitors for children has made EEG monitoring more popular.
Several studies have shown that monitoring EEG while under GA allows customization and titration of GA.
However, the usefulness of EEG monitoring in children have not been established.
It is a relatively new technology for some and will involve additional costs.
The investigators aim to understand the perceptions of participants regarding EEG monitoring during paediatric anaesthesia care by administering a survey before and after GA.
Study Overview
Status
Recruiting
Study Type
Observational
Enrollment (Estimated)
400
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Teddy S Fabila, Doctor of Medicine
- Phone Number: +65 6394 5861
- Email: teddy.fabila@kkh.com.sg
Study Locations
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-
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Singapore, Singapore, 229899
- Recruiting
- KK Women's and Children's Hospital
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Contact:
- Teddy S Fabila, Doctor of Medicine
- Phone Number: +65 6394 5861
- Email: teddy.fabila@kkh.com.sg
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Contact:
- Choon Looi Bong, Senior Consultant
- Phone Number: +65 6394 1073
- Email: bong.choon.looi@singhealth.com.sg
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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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
All parents of children 1-16 years old and patients 12-16 years old coming for elective surgery requiring GA at KK Women's and Children's Hospital.
Description
Inclusion Criteria:
- All parents of children 1-16 years old and patients 12-16 years old coming for elective surgery requiring GA at KK Women's and Children's Hospital will be invited to voluntarily participate in an electronic survey on Form SG.
Exclusion Criteria:
- Parents and patients coming for emergency surgery will not be invited for the survey.
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 |
|---|
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The study will include all parents of children aged one year and 16 yo and patients 12-16 yo
All parents of children 1-16 years old and patients 12-16 years old coming for elective surgery requiring GA at KK Women's and Children's Hospital will be invited to voluntarily participate in an electronic survey on Form SG.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Survey on patient and parental perceptions of EEG-monitoring during paediatric anaesthesia care
Time Frame: May 2022 until September 2025
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Parents and patients completed the survey forms.
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May 2022 until September 2025
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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)
May 1, 2022
Primary Completion (Estimated)
May 30, 2025
Study Completion (Estimated)
September 30, 2025
Study Registration Dates
First Submitted
April 15, 2025
First Submitted That Met QC Criteria
April 15, 2025
First Posted (Actual)
April 22, 2025
Study Record Updates
Last Update Posted (Actual)
April 27, 2025
Last Update Submitted That Met QC Criteria
April 22, 2025
Last Verified
March 1, 2025
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2022-2217
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
All collected IPD, all IPD that underlie results in a publication.
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
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.