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Clinical studies on antihypertensive drugs used for proteinuria and hypertension intended for the bevacizumab-treated patients

Clinical studies on antihypertensive drugs used for proteinuria and hypertension intended for the bevacizumab-treated patients - Study on the effectiveness of antihypertensive drugs on proteinuria and hypertension of bevacizumab-treated patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000034880
Enrollment
70
Registered
2018-12-01
Start date
2019-02-01
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

colorectal cancer

Interventions

Azilsartan Oral administration once a day(max 6 month) Amlodipine Oral administration once a day(max 6 month)

Sponsors

Iwate Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients diagnosed with colon cancer by histology or cytology 2) Patients who had metastasis / recurrence in the image confirmed 3) Patients who are receiving bevacizumab 4) Patients diagnosed with hypertension after bevacizumab administration 5) Patients scheduled to be treated by ARB or CCB 6) Patients with ECOG PS 0 to 2 7) Patients of age 20 years or older 8) Scheduled research subjects who received the notification Patients who received written consent from participants to participate in this study

Exclusion criteria

Exclusion criteria: 1) Patients who have continued therapy with bevacizumab for more than 3 months 2) Patients who show proteinuria at least once within 4 weeks before consent acquisition 3) Patients with renal dysfunction of eGFR less than 30 mL / min / 1.73 m 2 at the time of consent acquisition 4) Patients who have taken the following medications before consent acquisition: ARB, angiotensin II converting enzyme inhibitor, direct renin inhibitor, diuretic, CCB, alpha / beta antagonist 5) Patients with diabetes 6) Patients with cardiovascular disorders 7) Patients who may be pregnant or pregnant 8) Patients who are considered difficult to register in this study due to clinically problematic mental illness

Design outcomes

Primary

MeasureTime frame
Rate of decrease in proteinuria

Secondary

MeasureTime frame
Rate of decrease in systolic / diastolic blood pressure Biochemical examination (TP, Alb, AST, ALT, BUN, SCr, T-Bil, Na, K, Cl, Ca) Urinalysis (uTP, uAlb, uCr, uNa, urinary osmotic pressure) Serum and urinary ET-1, AT-2, VEGF-A Adverse event related antihypertensive

Countries

Japan

Contacts

Public ContactSatoru Nihei

Iwate Medical University Faculty of clinical pharmacy course

satoru.2hei@gmail.com019-613-7111

Outcome results

None listed

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