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Effect of telmisartan on patients with renal dysfunction

Effect of telmisartan on patients with renal dysfunction - JINNAGA

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000040875
Enrollment
100
Registered
2020-06-25
Start date
2009-03-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Chronic Kidney Disease

Interventions

telmisartan 20 mg for 4 weeks and up-titrating telmisartan to 40 mg at 4 weeks and continuing the same dose until 104 weeks telmisartan 20 mg for 4 weeks and up-titrating telmisartan to 40 mg at 4 wee

Sponsors

Nagasaki University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients are included if they are at least 20 years of age, chronic kidney disease stage 3-4 with estimated glomerular filtration rate of 15-60 ml/min/1.73 m2, receiving anti hypertensive therapy, and have sustained blood pressure control

Exclusion criteria

Exclusion criteria: heavy liver dysfunction and/or poor bile secretion, possibility of pregnancy or lactation, past history of hypersensitivity for telmisartan or its analogous drugs, nephrotic proteinuria, corticosteroids or immunosuppressant agents within the past 6 months, acute myocardial infarction within 6 months, congestive heart failure, cerebral infarction, transient ischemic attack, and renal artery stenosis

Design outcomes

Primary

MeasureTime frame
A composite of doubling serum creatinine, transition to chronic kidney disease stage 5, the onset of end-stage renal disease, or death from any causes within 104 weeks.

Secondary

MeasureTime frame
Amount of urinary protein, and decreased eGFR during the 104 weeks.

Countries

Japan

Contacts

Public ContactTomoya Nishino

Nagasaki University Hospital Nephrology

tnishino@nagasaki-u.ac.jp0958197282

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026