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Effectiveness of Candesartan and Telmisartan on Morning Hypertension in Japanese Obese Patients

A Randomized, Comparative Study of the Effects of Candesartan and Telmisartan on the Home Blood Pressure, Glucose and Lipid Metabolism in the Hypertensive Patients With the Accumulation of Visceral Fat by the Central Registration System

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00288717
Enrollment
300
Registered
2006-02-08
Start date
2006-02-28
Completion date
2007-09-30
Last updated
2007-01-11

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

Conditions

Hypertension

Brief summary

To investigate the effects of Candesartan and Telmisartan on the home blood pressure, glucose and lipid-metabolism in the hypertensive patients with the accumulation of visceral fat by the newly developed Tele-medicine system

Detailed description

A randomized, comparative study of the effects of Candesartan and Telmisartan on the home blood pressure, glucose and lipid metabolism in the hypertensive patients with the accumulation of visceral fat by the central registration system

Interventions

DRUGCandesartan
DRUGTelmisartan

Sponsors

Non-Profit Organaizaion LINE
CollaboratorUNKNOWN
Saitama Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Circumference at waist: male ≧85 cm, female ≧90 cm * Hypertensive patient with untreated hypertension, and casual blood pressure of systole ≧140 mmHg, or diastole ≧90 mmHg * Hypertensive patient with hypertension under treatment, and casual blood pressure of systole ≧130 mmHg, or diastole ≧85 mmHg

Exclusion criteria

* Significant hypertensive patient with diastolic blood pressure ≧120 mmHg * Malignant hypertensive patient * Patient with a contraindication to the study drugs (hypersensitivity, significant hepatic diseases, pregnant woman) * Patient with urinary protein (qualitative) +~++ * Patient with familial hyperlipidemia * Other patients judged as ineligible for the study

Design outcomes

Primary

MeasureTime frame
Home blood pressure in the early morning

Secondary

MeasureTime frame
M/E ratio
Casual blood pressure
Body fat percentage
Body weight
Height
BMI
Blood potassium
Total cholesterol
Home blood pressure at bedtime
LDL cholesterol
Triglyceride
Blood glucose
IRI
HbAlc*
HOMA-IR
Urinary trace albumin
Creatinine
HDL cholesterol

Countries

Japan

Contacts

Primary ContactHidetomo Nakamoto, MD
nakamo_h@saitama-med.ac.jp+81-0492-76-1258

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026