Title

Kagoshima Collaborate Trial in Metabolic Syndrome (KACT Study)
Effects of Valsartan on Metabolic Syndrome in Patients With Hypertension
  • Phase

    Phase 4
  • Study Type

    Interventional
  • Status

    Unknown status
  • Intervention/Treatment

    valsartan ...
  • Study Participants

    250
The purpose of this study is to consider the following points in patients with hypertension who complicated by metabolic syndrome for Valsartan basis treatment and an existing, standard treatment.

Blood pressure control
Changing of adiponectin and plasminogen activator inhibitor-1
Influence metabolizing and cardiac function, etc.
The primary endpoints are:

blood pressure control
Adiponectin and plasma type1 plasminogen active inhibitor

The secondary endpoints are

HOMA-IR
HbA1c
TNF-α
IL-6
Plasma B-type natriuretic peptide
LVMI
E/A ratio
Tei-index
Apo-J
Study Started
Jun 30
2006
Primary Completion
Dec 31
2009
Anticipated
Study Completion
Dec 31
2009
Anticipated
Last Update
Jun 03
2010
Estimate

Drug Valsartan

Valsartan 80 to 160 mg

Valsartan Active Comparator

Valsartan 80 to 160mg

standard therapy No Intervention

Criteria

Inclusion Criteria:

Out patients with hypertension male and female
Systolic blood pressure (SBP)≧140mmHg and/or diastolic blood pressure (DBP)≧90 mmHg
Waist Surrounding diameter male≧85cm female≧90cm
Patient who is treating either high triglyceride,low HDL,or diabetes mellitus
Patient who is untreatment high triglyceride blood syndrome and low HDL blood syndrome,diabetes mellitus is triglceride≧150mg/dl and/or HDL cholesterol < 40 mg/dl or fasting blood glucose ≧110 mg/dl
Untreated patients with hypertension,or patients is treated with antihypertensive agents except for ACE-I and ARB

Exclusion Criteria:

Patient who is using ACE-I and ARB
Serum creatinine ≧ 3 mg/dl
Liver impairment
History of allergy to valsartan
Pregnant women
Judgment by the physician that participation was unwise on the basis of patient characteristics and drug safety
No Results Posted