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NCT Number: NCT06727409

Use of Clinical-trials and Simulation Models to Estimate Cost-effectiveness of Non-steroidal Mineralocorticoid Antagonists, RASi and SGLT2i as Triple Therapy With Type 2 Diabetes and Chronic Kidney Disease

To evaluate triple therapy with nsMRA, RASi and SGLT2i on albuminuria in individuals with T2D and CKD

Recruiting

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Key information

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Adults aged 18 years or above
  • Diagnosis of type 2 diabetes at least 6 months
  • CKD (eGFR by CKD-EPI 25-90 ml/min/1.73m2 with uACR 30 to <300 mg/g) and/or those with severely elevated albuminuria (uACR 30-5000 mg/g) and eGFR > 60 ml/min/1.73m2.
  • Patients should have a serum potassium <4.8 mmol/l at screening
  • On SGLT2i (dapagliflozin or empaglifozin) at screening at stable doses for at least 4 weeks.
  • On ACEi or ARB at maximum tolerated dose per manufacturer's label that did not cause unacceptable side effects
  • In the opinion of the investigator, absence of any physical limitations, addictive diseases, or underlying medical conditions (including mental health) that may preclude the patient from being a suitable study candidate.

Exclusion criteria

  • Type 1 diabetes
  • Allergy, contraindications or intolerance to ACEi/ARB
  • Contraindications or intolerance to mineralocorticoid receptor antagonists
  • Allergy, contraindications to SGLT2is
  • Currently pregnant or planning pregnancy
  • HbA1c >9% at enrolment
  • Uncontrolled hypertension SBP > 160mmHg or hypotension <90 mmHg at enrolment
  • Concomitant therapy with eplenerone, spironolactone that cannot be discontinued.
  • History of stroke or worsening heart failure in the past 6 months prior to screening
  • Diabetic ketoacidosis, hyperosmolar hyperglycaemic state or myocardial infarction in the six months prior to screening
  • Patients on renal replacement therapy or likely require kidney transplant or dialysis during the study period
  • On concomitant strong CYP3A4 inhibitors that cannot be discontinued
  • Adrenal insufficiency
  • Currently participating in another investigational study protocol where the testing or results may interfere with study compliance, diagnostic results, or data collection.
  • An identified protected vulnerable patient (including but not limited to those in detention, or a prisoner).

Treatment and study plan

Finerenone

Drug

Finerenone 10mg or 20 mg as tolerated on top of maximal tolerated RASi and stable SGLT2i therapy

Primary outcomes

  1. Change in urine albumin creatinine ratio (uACR)

    Time frame: 26 weeks

    urine ACR between baseline and end of study (26 weeks)

Secondary outcomes

  1. Change in estimated glomerular filtration rate (eGFR)

    Time frame: 26 weeks

    eGFR calculated from plasma creatinine from baseline to end of study in ml/min/1.73m2

  2. Change in potassium

    Time frame: 26 weeks

    Change in plasma potassium (mmol/l) from baseline to end of study

  3. Change in blood pressure

    Time frame: 26 weeks

    Change in systolic and diastolic blood pressure (mmHg) from baseline to end of study

  4. Change in heath related quality of life

    Time frame: 26 weeks

    change in HRQoL from baseline to end of study using EQ5D

  5. Change in body weight

    Time frame: 26 weeks

    Change in body weight (kg) from baseline to end of study

Study contacts

Contact information is provided by the study sponsor or research team.

Elaine Chow

CONTACT

[email protected]

+852 35051641

Sponsors and collaborators

Lead sponsor

Chinese University of Hong Kong

Other

Registry information

Acronym: RAiSiN

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Dec 10, 2024
Registry last updated
Mar 5, 2025

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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