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Diet soda danger? study probes artificial sweeteners in teens with diabetes

NCT ID NCT03889522

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at how non-caloric artificial sweeteners (like those in diet drinks) affect body composition, metabolism, and blood sugar control in 21 youth aged 5-17 with type 1 diabetes. Researchers measured body fat and muscle using special scans and tested blood for markers of kidney and liver function, cholesterol, and blood sugar control. Participants also reported their intake of artificial sweeteners through questionnaires. The goal was to see if these sweeteners are linked to health risks in this group.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
non-caloric artificial sweeteners (dietary consumption)
What this could lead to
If results show a link, it could guide dietary recommendations for youth with type 1 diabetes to reduce future complication risks.
What could go wrong
This is a small, observational study with only 21 participants, so findings may not apply broadly. It only looks at associations, not cause and effect.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

21 people

The number who actually took part.

Started

May 2019

Finished

Feb 2021

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Youth receiving care at the Children's Hospital of Wisconsin Diabetes Clinic.

Ages

5 to 17 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Males and females aged 5-17 years with a clinical diagnosis of T1D of ≥ 6 months in duration 2. BMI between the 5th and 95th percentile Exclusion Criteria: 1. Presence of severe, active disease that requires the use of chronic medication, with the exception of well-controlled autoimmune thyroiditis/hypothyroidism or celiac disease that is well-controlled on a gluten free diet. 2. Diabetes other than T1D 3. Chronic illness known to affect glucose metabolism 4. Psychiatric impairment, with the exception of well-controlled depression or anxiety, that will affect the ability to participate in the study 5. Female participants of child-bearing age with reproductive potential must not be knowingly pregnant 6. Any condition that, in the investigator's opinion, may compromise study participation or may confound the interpretation of the study results

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Medical College of Wisconsin

    Milwaukee, Wisconsin, 53226, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.