Type 2 Diabetes Trial, Recruiting NCT06838416 Sponsor: Second Affiliated Hospital of Soochow University Condition: Type 2 Diabetes
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Type 2 Diabetes Trial, Recruiting

NCT06838416
Recruiting Not Applicable

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 23 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

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

Status
Recruiting
Phase
Not Applicable
Sponsor
Second Affiliated Hospital of Soochow University
Registry
ClinicalTrials.gov
Start date
17 November 2023
Est. completion
31 December 2025

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Change in Urine Albumin-to-Creatinine Ratio (UACR)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov