Unique ID issued by UMIN | UMIN000005684 |
---|---|
Receipt number | R000003692 |
Scientific Title | Prospective, randomized, open-label,clinical trial comparing the effects of olmesartan/azelnidipine and candesartan/amlodipine on blood pressure, endothelial function and makers for obesity/oxidative stress/chronic kidney diseases |
Date of disclosure of the study information | 2011/06/01 |
Last modified on | 2017/03/20 09:44:36 |
Prospective, randomized, open-label,clinical trial comparing the effects of olmesartan/azelnidipine and candesartan/amlodipine on blood pressure, endothelial function and makers for obesity/oxidative stress/chronic kidney diseases
Prospective, randomized, open-label,clinical trial comparing the effects of olmesartan/azelnidipine and candesartan/amlodipine
Prospective, randomized, open-label,clinical trial comparing the effects of olmesartan/azelnidipine and candesartan/amlodipine on blood pressure, endothelial function and makers for obesity/oxidative stress/chronic kidney diseases
Prospective, randomized, open-label,clinical trial comparing the effects of olmesartan/azelnidipine and candesartan/amlodipine
Japan |
Hypertension
Cardiology |
Others
NO
Prospective, randomized, open-label,clinical trial comparing the effects of olmesartan/azelnidipine and candesartan/amlodipine on blood pressure, endothelial function and makers for obesity/oxidative stress/chronic kidney diseases
Efficacy
Phase IV
Blood pressure (On visit/Home monitoring)
Ambulatory blood pressure monitoring
Eight weeks after administration
Markers indicating obesity (e.g. adiponectin), inflammation (high sensitive CRP), oxidative stress (8-OHdG/ MDA-LDL), early-staged kidney diseases (microalbuminuria)
Eight weeks after administration
Interventional
Cross-over
Randomized
Individual
Open -but assessor(s) are blinded
Active
2
Treatment
Medicine |
Administration of olmesartan/azelnidipine
Administration of
candesartan/amlodipine
20 | years-old | < |
75 | years-old | > |
Male and Female
1) Hypertensive patients with administration of normal dosage of ARB who did not reach
the recommendation of Hypertension Guidelines issued by Japanese Association of Hypertension
2) Outpatients
3) Subjects who gave written informed consent
1) Allergy against olmesartan/candesartan/azelnidipine/amlodipin
2) Poor-controlled hypertension (DBP>110 mmHg)
3) Poor-controlled diabetes (HbA1c>8.0 %)
4) Secondary hypertension
5) History of stroke, acute coronary syndrome or any cardiovascular diseases needed for inpatient-treatments within 6 months
6) Either level of aspartate aminotransaminase or alanine aminotransferase exceeds three-fold of the normal limits.
7) End stage renal disease
8) Symptomatic (NYHA III or IV) congestive heart failure
9) Malignancies or other diseases with poor prognosis
10) Pregnant
11) Subjects whose doctor in charge do not agree to join the trial
30
1st name | |
Middle name | |
Last name | Katsunori Ikewaki |
National Defense Medical College
Department of Internal Medicine I
3-2 Namiki, Tokorozawa, JAPAN 359-8513
04-2995-1597
katsunorike@ndmc.ac.jp
1st name | |
Middle name | |
Last name | Makoto Ayaori |
National Defense Medical College
Department of Internal Medicine I
3-2 Namiki, Tokorozawa, JAPAN 359-8513
04-2995-1597
ayaori@ndmc.ac.jp
National Defense Medical College
Foundation for Promotion of Defense Medicine
Non profit foundation
Japan
NO
防衛医科大学校
2011 | Year | 06 | Month | 01 | Day |
Unpublished
Terminated
2010 | Year | 02 | Month | 01 | Day |
2010 | Year | 02 | Month | 01 | Day |
2012 | Year | 01 | Month | 01 | Day |
2011 | Year | 05 | Month | 31 | Day |
2017 | Year | 03 | Month | 20 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000003692