Tartu University Hospital
Tartu, Estonia
NCT Number: NCT04151849
The primary aim of this observational study is to describe the effects of glucagon-like peptide-1 (GLP-1) receptor agonists and Sodium-Glucose Co-transporter 2 inhibitors ( SGLT-2 inhibitors) on adrenal function. Secondary endpoint is change in intestinal microbiota.
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Notify Me18 year and older
All sexes
Observational
Tartu, Estonia
This is an observational study conducted in patients with type 2 diabetes starting treatment with either GLP-1 receptor agonist or sodium-glucose cotransporter-2 (SGLT-2) inhibitor.
Planned study cohort consists of 60 patients: 30 patients starting GLP-1 receptor agonist treatment and 30 patients starting SGLT-2 inhibitor treatment. All patients must have metformin as background therapy. All other diabetes medications are allowed.
Patients are tested before starting treatment, at 1 month (stool sample only), 3 months and 12 months after starting treatment. The primary endpoint is change in overnight urinary aldosterone corrected for creatinine.
Secondary endpoint is change in intestinal microbiota composition.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Treatment with GLP-1 agonist for up to 1 year.
Treatment with SGLT2 inhibitor for up to 1 year
Time frame: 3 months
Overnight urinary aldosterone compared to pretreatment level.
Time frame: At 1 month after starting treatment, at 3 months and 12 months.
Fecal microbiota will be compared to pre-treatment sample.
Time frame: 12 months
Overnight urinary aldosterone at 12 months compared to pretreatment level.
Time frame: At 3 months and 12 months.
Change in adrenocorticotropic hormone in serum compared to pretreatment level.
Time frame: At 3 months and 12 months.
Change in plasma cortisol compared to pretreatment level
Time frame: At 3 months and 12 months.
Change in overnight urinary cortisol compared to pretreatment level.
Time frame: At 3 months and 12 months.
Change in plasma aldosterone compared to pretreatment level.
Time frame: At 3 months and 12 months.
Change in plasma renin compared to pretreatment level.
Time frame: At 3 months and 12 months.
Change in serum sodium compared to pretreatment level.
Time frame: At 3 months and 12 months.
Change in serum potassium compared to pretreatment level.
Time frame: At 3 months and 12 months.
Change in glycated hemoglobin A1c compared to pretreatment level.
Time frame: At 3 months and 12 months.
Change in plasma ceruloplasmin compared to pretreatment level.
Time frame: At 3 months and 12 months.
Change in plasma ferritin compared to pretreatment level.
University of Tartu
Other
Complementary Effects of New Diabetes Medications on Adrenal Function and Intestinal Microbiota
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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