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Goal-Directed Therapy to Reduce Kidney and Cardiovascular Risk in Diabetic Kidney Disease (GOLD-STANDARD)

Goal-Directed Therapy to Reduce Kidney and Cardiovascular Risk in Diabetic Kidney Disease (GOLD-STANDARD)

Recruiting
18 years and older
All
Phase N/A

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Overview

GOLD-STANDARD is a pragmatic, open-label pilot randomized controlled trial evaluating the feasibility, safety, and implementation of an early goal-directed Cardio-Kidney-Metabolic (CKM) care strategy compared with usual care in adults with type 2 diabetes and diabetic kidney disease who are at increased cardiovascular risk. Participants will be followed for 12 months to assess treatment uptake, adherence, retention, and safety outcomes, and to inform the design of a future definitive trial.

Description

The GOLD-STANDARD study will evaluate the feasibility of an early, goal-directed Cardio-Kidney-Metabolic (CKM) care strategy that integrates kidney, cardiovascular, and metabolic risk management within routine nephrology practice. Using a pragmatic randomized design, the study will assess whether a structured approach to CKM care can be implemented safely and effectively within Ontario's healthcare system.

The primary objective of this pilot study is to evaluate feasibility, including recruitment, retention, treatment implementation, and adherence. Safety and treatment uptake measures will also be assessed over 12 months of follow-up. Findings from this study will inform the design and conduct of a future large-scale trial evaluating the impact of early CKM care on clinical kidney and cardiovascular outcomes.

Eligibility

Inclusion Criteria

  1. Age ≥ 18 years
  2. T2DM
  3. CKD (eGFR ≥ 25-60 mL/min/1.73 m² OR UACR ≥ 30 mg/g) - on screening labs
  4. High Cardiovascular (CV) Risk: Defined as a history of prior myocardial infarction (MI), stroke, or peripheral artery disease (PAD), or the presence of cardiovascular risk factors, (specifically age 40 years or older and at least one of the following: cholesterol above target (LDL≥1.8 mmol/L OR on cholesterol lowering medication - within past 24 months), hypertension (≥130/80 mmHg or on BPLMs), or atrial fibrillation.)
  5. Open to start new medications

Exclusion Criteria:

  1. Type 1 diabetes
  2. HbA1c ≥10% within past 12 months
  3. Serum potassium ≥ 5.2 mmol/L on screening labs
  4. Baseline Blood Pressure (BP) \< 100/60 mmHg at screening
  5. Treated with new or intensified immunosuppression therapy for new (or relapse/flare of pre-existing) kidney disease within the last 60 days
  6. Kidney Transplant
  7. In the opinion of the investigator, currently treated with maximum tolerated dose of ≥3 medication classes:: RASi, SGLT2i, nsMRA or GLP1RA
  8. Currently prescribed all 4 medication classes : RASi, SGLT2i, nsMRA or GLP1RA
  9. Intolerance or allergy to any of RASi, SGLT2i, nsMRA or GLP1RA
  10. Known Heart Failure with Reduced Ejection Fraction (HFrEF)
  11. Current pregnancy, lactation or women of childbearing potential, unless using highly effective contraception

Study details
    Diabetic Kidney Disease (DKD)
    Type 2 Diabetes Mellitus (T2DM)
    Chronic Kidney Disease

NCT07434791

Sunnybrook Health Sciences Centre

20 October 2026

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