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NCT Number: NCT04151849

Effects of Diabetes Medications on Adrenal Function and Intestinal Microbiota

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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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Tartu University Hospital

Tartu, Estonia

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age > 18 years
  • Type 2 diabetes
  • HbA1c < 10%
  • BMI >32
  • Daily dose of metformin 1,5 g or more.
  • No change in diabetes treatment at least 90 days before starting the study.
  • Never used SGLT-2 inhibitors or/and GLP-1 receptor agonist.
  • Tested negative to glutamic acid decarboxylase 65 autoantibodies.

Exclusion criteria

  • Pregnancy and lactation.
  • Use of systemic antibiotic treatment < 60 days before starting the study.
  • Use of spironolactone < 60 days before starting the study.
  • Use of oral contraceptives or hormonal replacement therapy.
  • Use of immunosuppressive drug
  • Heart failure New York Heart Association III-IV
  • Severe liver disease.
  • Malignant disease.

Treatment and study plan

GLP-1 receptor agonist

Drug

Treatment with GLP-1 agonist for up to 1 year.

SGLT2 inhibitor

Drug

Treatment with SGLT2 inhibitor for up to 1 year

Primary outcomes

  1. Urinary aldosterone at 3 months

    Time frame: 3 months

    Overnight urinary aldosterone compared to pretreatment level.

Secondary outcomes

  1. Change in gastrointestinal microbiota.

    Time frame: At 1 month after starting treatment, at 3 months and 12 months.

    Fecal microbiota will be compared to pre-treatment sample.

  2. Urinary aldosterone at 12 months

    Time frame: 12 months

    Overnight urinary aldosterone at 12 months compared to pretreatment level.

Other outcomes

  1. Serum adrenocorticotropic hormone

    Time frame: At 3 months and 12 months.

    Change in adrenocorticotropic hormone in serum compared to pretreatment level.

  2. Plasma cortisol

    Time frame: At 3 months and 12 months.

    Change in plasma cortisol compared to pretreatment level

  3. Urinary cortisol

    Time frame: At 3 months and 12 months.

    Change in overnight urinary cortisol compared to pretreatment level.

  4. Plasma aldosterone

    Time frame: At 3 months and 12 months.

    Change in plasma aldosterone compared to pretreatment level.

  5. Plasma renin

    Time frame: At 3 months and 12 months.

    Change in plasma renin compared to pretreatment level.

  6. Serum sodium

    Time frame: At 3 months and 12 months.

    Change in serum sodium compared to pretreatment level.

  7. Serum potassium

    Time frame: At 3 months and 12 months.

    Change in serum potassium compared to pretreatment level.

  8. Glycated hemoglobin A1c

    Time frame: At 3 months and 12 months.

    Change in glycated hemoglobin A1c compared to pretreatment level.

  9. Ceruloplasmin

    Time frame: At 3 months and 12 months.

    Change in plasma ceruloplasmin compared to pretreatment level.

  10. Ferritin

    Time frame: At 3 months and 12 months.

    Change in plasma ferritin compared to pretreatment level.

Sponsors and collaborators

Lead sponsor

University of Tartu

Other

Registry information

Official study title

Complementary Effects of New Diabetes Medications on Adrenal Function and Intestinal Microbiota

Important dates

Study start
2019
Primary completion
2023
Study completion
2023
First posted
Nov 5, 2019
Registry last updated
Feb 21, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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