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FastingNCT06915493

Blood Glucose Levels in Children During Anesthesia

An observational study of Fasting, run by Landspitali University Hospital at 1 site in Iceland.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This cross-sectional study aims to investigate blood glucose levels in children during general anesthesia and explore the incidence of hypoglycemia after anesthesia induction in relation to preoperative fasting. Read more about this study

Who is it for?
Ages 1 day to 17 years
Conditions the study is for
Fasting
What is being tested?
General Anesthesia
How many people
350 participants
Where
1 siteIceland
Study dates
1 Oct 2023to 3 Mar 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 1 day to 17 years
  • All sexes
  • No healthy volunteers
  • Child

Study population: Convenience sample of children undergoing elective intervention under general anesthesia at Landspítali, the University Hospital of Iceland.

Who may be able to join

  • Children under 18 years of age who undergo intervention under general anesthesia. The parent or guardian understands and speaks Icelandic.

Who cannot join

  • Coexisting disease or treatment that may affect fasting blood glucose level; Preoperative intravenous fluid administration; Beta-blockers; Insulin and corticosteroids, endocrine disorders, acute pain, and emergency interventions.

Trial locations and contacts

1 site in 1 country.

Iceland1 site
  • Anesthesia Department Landspitali UH

    Reykjavik, 101

Other trials in Iceland

About this study

Official title: Blood Glucose Levels in Children During Anesthesia: Incidence of Hypoglycemia During Anesthesia Induction and Its Relationship to Preoperative Fasting

This cross-sectional study aims to investigate blood glucose levels in children during general anesthesia and explore the incidence of hypoglycemia after anesthesia induction in relation to preoperative fasting.

Blood glucose will be measured following anesthesia induction and prior to discontinuing the administration of the anesthetic agent.

Read the detailed description

This cross-sectional study aims to investigate blood glucose levels in children < 18 years during general anesthesia, and explore the incidence of hypoglycemia after anesthesia induction in relation to preoperative fasting.

The purpose is to evaluate whether guidelines for shortening the preoperative fasting period of children at our hospital have resulted in a shorter fasting duration and prevalence of low blood glucose levels during anesthesia induction. Also to shed light on blood glucose levels during general anesthesia and its correlation with intravenous fluid management and administration of steroidal anti-emetics.

Blood glucose sampling will be obtained and measured following anesthesia induction and prior to discontinuing the anesthetic agent. If general anesthesia lasts longer than one hour, additional blood glucose analysis will be conducted one hour after the first measurement.

Conditions
Fasting
Being tested
General Anesthesia
Keywords
Pediatrics, Children, General anesthesia, Preoperative fasting, Fasting blood glucose, Hypoglycemia
Medical subject headings
Fasting, Hypoglycemia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • General AnesthesiaOther

    Blood glucose measurements during general anesthesia

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Serum blood glucose level

    Blood glucose sampling and measured during general anesthesia

    Measured: Immediately/within five minutes after anesthesia induction and prior to discontinuing the anesthesia administration.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Apr 2025
  2. Study start1 Oct 2023
  3. Primary completion3 Mar 2025
  4. Study completion3 Mar 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
350 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06915493
Sponsor's protocol ID
47/2023
Status last verified
Apr 2025
First submitted
31 Mar 2025
Last updated
11 Apr 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes

Questions about this trial

What is this clinical trial studying?

An observational study of Fasting, run by Landspitali University Hospital at 1 site in Iceland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 11 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Iceland. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Serum blood glucose level (time frame: Immediately/within five minutes after anesthesia induction and prior to discontinuing the anesthesia administration.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Apr 2025.

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