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The Evaluation of Effects against Acute- or Relapse Infarction in Patients with both Diabetes and Hypertension Taking ARB and PPAR-gammma Inhibitor

The Evaluation of Effects against Acute- or Relapse Infarction in Patients with both Diabetes and Hypertension Taking ARB and PPAR-gammma Inhibitor - The Evaluation of Effects against Acute- or Relapse Infarction in Patients with both Diabetes and Hypertension Taking ARB and PPAR-gamma Inhibitor (ARITA Study)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000001548
Enrollment
200
Registered
2008-12-03
Start date
2008-05-01
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

Patients with diabetes and hypertension

Interventions

In the thiazolidine derivatives group, thiazolidine derivatives will be prescribed as per specifications attached. In sulfonylurea hypoglycemic agent, the agent will be prescribed as per specification

Sponsors

HuBit genomix, Inc.
Lead Sponsor
National Cerebral and Cardiovascular Center
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patient with both diabetes and essential hypertension or patient undergoing treatment of antihypertensive agent who is newly taking diabetic medicine

Exclusion criteria

Exclusion criteria: 1) History of cardiac failure 2) Diagnosis of Cardiovascular disturbance and/or cerebrovascular disease within 6 months 3) Secondary hypertension 4) Type I diabetes 5) Diagnosis and/or treatment of cancer within 5 years 6) Renal dysfunction 7) Liver dysfunction 8) History of side effects of TDZ or ARB 9) No current or past history of psychiatric disorders 10) Pregnant women or lactating mothers 11) Participating another clinical investigation within 3 months 12) Patients judged by the investigator to be unfit to be enrolled into the study

Design outcomes

Primary

MeasureTime frame
Primary end-point is time from randomization to first occurrence of any of the events in the following composite: 1. Cardiovascular disturbance 2. Cerebrovascular disease 3. Renal failure 4. Administration of dialysis treatment 5. Cardiac mortality 6. Cerebrovascular mortality

Secondary

MeasureTime frame
Secondary end-point is time from randomization to first occurrence of any of the events in the following composite: 1. All-cause mortality 2. Cardiac depression and impairing renal function 3. Progression of diabetes 4. Progression of hypertension

Countries

Japan

Contacts

Public ContactYasuhiko Koezuka

HuBit genomix, Inc. Research & Development Department

ykoezuka@hubitgenomix.com03-5148-3992

Outcome results

None listed

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