Sugar vs. sweetener showdown: which is better for your blood sugar?
NCT ID NCT07656298
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compares how natural sugar (sucrose) and the artificial sweetener sucralose affect blood sugar control and metabolism in 120 adults with normal weight, overweight, or obesity. Participants will consume low or high doses of each sweetener in solid or liquid form over 12-week periods. The goal is to see if responses differ by body weight, dose, or how the sweetener is consumed.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- sucrose (natural sugar) and sucralose (artificial sweetener)
- What this could lead to
- If successful, this could clarify whether artificial sweeteners are better or worse for metabolism than natural sugar, and how dose and form (solid vs. liquid) matter.
- What could go wrong
- This is an early-stage observational study with only 120 participants, so results may not apply to everyone. It measures short-term effects, not long-term health outcomes.
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.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
About 120 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
-
Jul 2026
An estimate. Start dates often move.
- Expected to finish
-
Sep 2027
An estimate. End dates often move.
- 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.
- Ages
-
18 to 65 years
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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: * Adults aged 18 to 65 years at the time of enrollment. * Body Mass Index (BMI) between 18.5 and 39.9 kg/m². * Men and women who report a preference for sweet taste and habitual consumption of sugar and/or sweeteners. * Individuals in good general health, as determined by: 1. Medical history and clinical evaluation; 2. Absence of uncontrolled chronic diseases, such as diabetes, metabolic syndrome, severe hypertension, or advanced liver or renal disease; and 3. Baseline biochemical parameters within normal reference ranges, including fasting plasma glucose \<100 mg/dL, HbA1c \<5.7%, normal liver and renal function (ALT/AST and creatinine within reference ranges), and blood pressure \<140/90 mmHg without pharmacological treatment. * Less than 4 hours per week of moderate-to-vigorous physical activity. * Not following special or restrictive diets (e.g., ketogenic, strict vegetarian, or vegan diets). * Not taking medications known to affect metabolism, including, for example, antidiabetic drugs, systemic corticosteroids, weight-loss medications, or high-dose antioxidant supplements, except for stable use of hormonal contraceptives. * Willingness to maintain habitual diet and physical activity throughout the study, with the only modification being the assigned sweetener intervention. * Ability and willingness to comply with all study procedures and scheduled visits. * Provision of written informed consent before participation. Exclusion Criteria: * Gastrointestinal disorders influencing digestion or nutrient absorption (e.g., inflammatory bowel disease, celiac disease, malabsorption syndromes). * History of cancer not in remission. * Uncontrolled thyroid disorders. * History of bariatric surgery or extreme weight loss within the past 12 months. * Pregnancy, breastfeeding, or planning pregnancy during the study period. * Acute illness, major infection, hospitalization, or major surgery within the previous 6 months. * Any condition that, in the investigators' judgment, could compromise participant safety, protocol adherence, or interpretation of the study results.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Glucose metabolism are added.
Genom att skicka in godkänner du våra Användarvillkor
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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Hospital Universitario Virgen de la Victoria
RECRUITINGMálaga, Malaga, 29103, Spain
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a brazilian diet calm menopause hot flashes?
- Can a glucose monitor personalize weight loss for students?
- Mushrooms and a repurposed antidepressant: a new recipe for weight loss?
- Can a damaged kidney change how a drug works?
- Can a new injection help tackle obesity? a trial puts MWN105 to the test
- Oral pill aims to keep weight off after initial loss