World Health Organization site
Skip Navigation Links

Main
Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: JPRN
Last refreshed on: 17 October 2023
Main ID:  JPRN-UMIN000007705
Date of registration: 09/04/2012
Prospective Registration: No
Primary sponsor: Chiba University Hospital
Public title: The effects of AT1 receptor blocker (telmisartan) on serum lipid with hypertensive patients associated with multiple risk factors for cardiovascular disease
Scientific title: The effects of AT1 receptor blocker (telmisartan) on serum lipid with hypertensive patients associated with multiple risk factors for cardiovascular disease - The effects of telmisartan on serum lipid
Date of first enrolment: 2011/09/01
Target sample size: 30
Recruitment status: Recruiting
URL:  https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000009085
Study type:  Interventional
Study design:  Single arm Non-randomized  
Phase:  Not selected
Countries of recruitment
Japan
Contacts
Name:     minoru takemoto
Address:  1-8-1 Inohana, Chuo-ku, Chiba-shi, Chiba 260-8670, Japan Japan
Telephone: 043-222-7171
Email: minoru.takemoto@faculty.chiba-u.jp
Affiliation:  Chiba University Hospital Department of Medicine, Division of Diabetes, Metabolism and Endocrinology
Name:     Minoru Takemoto
Address:  1-8-1 Inohana, Chuo-ku, Chiba-shi, Chiba 260-8670, Japan Japan
Telephone: 043-222-7171
Email: minoru.takemoto@faculty.chiba-u.jp
Affiliation:  Chiba University Hospital Department of Medicine, Division of Diabetes, Metabolism and Endocrinology
Key inclusion & exclusion criteria
Inclusion criteria:
Exclusion criteria: The exclusion criteria were an age >70 years, current history of myocardial infarction and/or cerebral stroke, uncontrollable hypertension (diastolic pressure > 180mmHg) and hyperglycemia (HbA1c > 9.0%), renal failure (serum creatinin > 3.0mg/dL), abnormal liver or muscle enzymes (ALT>100 or ALT>100), patients who applied for other clinical trial within 3 months, expectant mother, lactating woman, patients who had taken ACE-I, thiazolidine and fibrate, inappropriate patients judged by the physician in charge

Age minimum: 20years-old
Age maximum: 70years-old
Gender: Male and Female
Health Condition(s) or Problem(s) studied
Diabetes Mellitus
Intervention(s)
Administration of Telmisartan or Telmisartan /Ca antagonist combination drug
Primary Outcome(s)
Serum lipid (low density lipoprotein cholesterol)
Secondary Outcome(s)
Secondary ID(s)
Source(s) of Monetary Support
None
Secondary Sponsor(s)
Ethics review
Status: YES
Approval date:
Contact:
Results
Results available: Yes
Date Posted:
Date Completed: 01/03/2014
URL:
Disclaimer: Trials posted on this search portal are not endorsed by WHO, but are provided as a service to our users. In no event shall the World Health Organization be liable for any damages arising from the use of the information linked to in this section. None of the information obtained through use of the search portal should in any way be used in clinical care without consulting a physician or licensed health professional. WHO is not responsible for the accuracy, completeness and/or use made of the content displayed for any trial record.
Copyright - World Health Organization - Version 3.6 - Version history