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Dapagliflozin in patients with chronic kidney disease

Dapagliflozin in patients with chronic kidney disease - DAPA-NS

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083690
Enrollment
Unknown
Registered
2024-04-30
Start date
2024-05-01
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

chronic kidney disease

Interventions

Experimental Group:Dapagliflozin 10mg qd
Control group:Blank control

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Chronic kidney disease (abnormal renal structure or function: proteinuria, abnormal urinary sediment, renal tubule-related lesions, abnormal histological examination and abnormal imaging examination) for more than 3 months; 2. Patients diagnosed with chronic kidney disease (including nephrotic syndrome or nephritic syndrome) in the Department of Nephrology of our hospital; 2. Aged from 18 to 80 years old; 3. Take dapagliflozin regularly; 4. 24-hour urinary protein =150mg/24h; 5. Use stable doses of an angiotensin-converting-enzyme inhibitor (ACEi) or angiotensin-receptor blocker (ARB) for longer than 1 week.

Exclusion criteria

Exclusion criteria: 1. Severe liver dysfunction; 2. Severe renal impairment, eGFR=15 mL/min/1.73m2; 3. Urinary tract infection; 4. Osteoporosis; Type 5.1 or type 2 diabetes mellitus, polycystic kidney disease, lupus nephritis, or ANCA-associated vasculitis; 6. The presence of events that may affect the follow-up, such as the presence of malignant tumors, drug or alcohol abuse, severe respiratory diseases; 7. Exclude patients with severe mental disorders.

Design outcomes

Primary

MeasureTime frame
Plasma drug concentrations;

Secondary

MeasureTime frame
Urinary Drug concentration;

Countries

China

Contacts

Public ContactHui Zhong

West China Hospital of Sichuan University

medzhonghui@163.com+86 189 8060 1215

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026