Chronic Kidney Disease Trial, Recruiting NCT07481526 Sponsor: AstraZeneca Condition: Chronic Kidney Disease
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Chronic Kidney Disease Trial, Recruiting

NCT07481526
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 aged 18 years or older, of any gender.
  • People who are willing and able to sign a written consent form to take part in the study.
  • People with a confirmed diagnosis of chronic kidney disease (CKD), shown by either reduced kidney function lasting at least 3 months, or signs of kidney damage (such as protein in the urine, abnormal kidney imaging, or kidney biopsy results) lasting at least 3 months (confirm with trial site for exact measurements).

Who may not be able to join:

  • People with a serious life-threatening illness where life expectancy is less than 2 years.
  • People with severe heart conditions, including dangerous heart rhythm problems, or a major heart or stroke event (such as a heart attack, stroke, or heart-related death) within the past 3 months.
  • People who are currently pregnant or breastfeeding.
  • People who are currently taking part in another clinical trial, or who have received an experimental treatment within the past 3 months.
  • People whose primary condition at the time of joining is end-stage kidney disease, kidney replacement therapy (such as dialysis), sudden (acute) kidney injury, or a kidney condition that has been present for 3 months or less.

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 21 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: Xiao Qiang Ding, Zhongshan Hospital Affiliated with Fudan University

Phone: 1-877-240-9479

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
Registry
ClinicalTrials.gov
Start date
27 February 2026
Est. completion
30 December 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Proportion of CKD patients with HP, HF, HTN, and HK at baseline, respectively; Adoption rate of medications (e.g., Endothelin receptor antagonists [ERA], MRA, RASi, SGLT2i); Clinical indicators for CKD patients and CKD patients with HP, HF, HTN, or HK; Clinical outcomes of CKD patients and CKD patients with HP,HF,HTN,or HK; Clinical outcomes of CKD patients and CKD patients with HP,HF,HTN,or HK; Clinical outcomes of CKD patients and CKD patients with HP,HF,HTN,or HK; Clinical outcomes of CKD patients and CKD patients with HP,HF,HTN,or HK; Clinical outcomes of CKD patients and CKD patients with...

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: 21 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