NCT Number: NCT00330785
Open Label Study Assessing Effectiveness Of Amlodipine/Atorvastatin In Subjects With Hypertension and Dyslipidaemia
To evaluate the effectiveness of amlodipine/atorvastatin therapy by assessing the percentage of subjects who reach target blood pressure (BP) and LDL-C targets as defined by their governing guidelines.
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Notify MeKey information
Conditions
Age range
18 year–80 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 3
Primary location
Pfizer Investigational Site, Calgary, Alberta, Canada
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Patients who are above target LDL-C and BP who are eligible for treatment
Exclusion criteria
- High liver enzymes
Treatment and study plan
Primary outcomes
-
To evaluate the number of patients who reach target blood pressure (BP) and
-
LDL-C targets as defined by their governing guidelines.
Secondary outcomes
-
To assess changes from baseline to end of treatment for the following efficacy
-
parameters: LDL-C, total cholesterol (TC), triglycerides, high-density lipoprotein
-
cholesterol (HDL-C), HDL-C/LDL-C ratio, TC/HDL-C ratio. Systolic Blood Pressure
-
(SBP) and Diastolic Blood Pressue (DBP).
Sponsors and collaborators
Lead sponsor
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
Industry
Registry information
Official study title
An International, Multicentre, Open Label Study To Assess The Effectiveness Of Amlodipine -Atorvastatin Combination In Subjects With Hypertension and Dyslipidaemia. (The JEWEL Study)
Acronym: JEWEL I
Important dates
- Study start
- 2004
- Study completion
- 2005
- First posted
- May 29, 2006
- Registry last updated
- Jan 27, 2021
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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