Type 2 Diabetes Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have been diagnosed with Type 2 diabetes, based on the 1999 World Health Organization diagnostic guidelines
- People who are 18 years of age or older
- People whose urine and kidney function tests show a certain level of protein in the urine (UACR of 30 mg/g or more) and adequate kidney filtering ability (eGFR of 30 ml/min/1.73 m² or more), both present for more than 3 months
- People who have been taking a stable dose of a specific type of blood pressure medication (ARB or ACEI) for at least 4 weeks before joining the trial
- People who are willing to sign a consent form and follow the study's requirements
Who may not be able to join:
- People whose kidney disease was diagnosed before their Type 2 diabetes
- People with a high potassium level in their blood (above 4.8 mmol/L)
- People whose blood pressure is not well controlled at the screening visit (top number of 160 mmHg or more, and/or bottom number of 100 mmHg or more, based on an average of three measurements lying down)
- People whose blood sugar control is poor, with an HbA1c (a measure of average blood sugar over roughly 3 months) above 9%
- People with an active urinary tract infection or other conditions that could affect urine test results
- People with a condition where the adrenal glands do not work properly (primary or secondary adrenal insufficiency)
- People currently taking a type of medication called mineralocorticoid receptor antagonists
- People who have taken certain medications known to affect kidney protein levels or kidney filtering ability within the past 4 weeks (with some exceptions — confirm with trial site)
- People taking certain strong medications that affect how the body processes drugs (strong CYP3A4 inhibitors), including itraconazole, ketoconazole, ritonavir, nelfinavir, cobicistat, clarithromycin, telithromycin, nefazodone, or carbamazepine
- People with significantly elevated liver enzyme or bilirubin levels in their blood tests (above thresholds set by the trial — confirm with trial site)
- People who have used systemic steroid medications (such as oral, intravenous, or joint-injected corticosteroids) for more than 7 days in the 12 weeks before screening, or who have used them or needed immune-suppressing treatment in the past 14 days
- People who have had any type of cancer in the past 5 years, whether or not it has been treated
- People who are pregnant, breastfeeding, planning to become pregnant soon, or not using adequate contraception
- People who have taken part in another interventional clinical trial within the 3 months before screening
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Xie Ying, Ph.D., Second Affiliated Hospital of Suzhou University
Phone: 13962187062
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Change in Urine Albumin-to-Creatinine Ratio (UACR)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.