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Summary: Novartis Pharmaceuticals Corporation is conducting
a clinical research study for the treatment of high blood pressure.
This study evaluates the effectiveness and safety of an investigational
drug in combination with an FDA approved drug for the treatment
of patients with high blood pressure. The study will examine if
the combination of the investigational drug and FDA approved drug
lowers blood pressure as much as the FDA approved drug does alone.
Participants must meet the following criteria:
Must be 18 years of age or older
Must have a doctors diagnosis of high blood pressure
Must have diastolic blood pressure (lower number) less
than 110
Patients will be excluded from the studies for any of the following
reasons:
History of malignancy including leukemia and lymphoma (but
not basal cell skin cancer) within the past 5 years
Experienced a heart attack, stroke, or by-pass surgery
in the last 12 months
Women who are pregnant or breast-feeding
Experienced inflammatory bowel disease within the last
12 months or had gastrointestinal surgery
Current diagnosis of congestive heart failure
Type 1 or Type 2 diabetes mellitus with glycosylated hemogloving
(HbA1c)>9% at Visit 1.
For additional information about this study, Contact:
Irit Steiner, Study Coordinator
Richard M. Levy, MD
3580 California Street, #302
San Francisco, CA 94118
Telephone: 415-929-9405
Fax: 415-929-1307
Summary: Novartis is conducting a 10-12 week clinical research
study to find out if the combination of two FDA approved study
drugs will be safe and effective in treating patients for both
high blood pressure and cholesterol.
This study should provide efficacy, tolerability, and safety data
for the high dose of the combination of two FDA approved study
drugs indicated for high blood pressure and high cholesterol.
We hope to confirm that the study drugs given in combination are
as safe and effective as given alone.
Participants must meet all of the following criteria:
Be 18-75 years of age with both high blood pressure and
high cholesterol
Female patients must not be pregnant or lactating and must
agree to use acceptable forms of birth control
Must be on a stable moderate to high dose of an approved
statin drug for the past 3 months (examples: Meyacor, Zocor, Prayachol,
Lescol, Lipitor, Crestor)
Participants will be excluded from the studies for any of the
following reasons:
History of major gastrointestinal tract surgery or experienced
inflammatory bowel disease within the last 12 months
History of cancer including leukemia and lymphoma (excluding
basal cell skin cancer) within the past 5 years
Diabetic patients requiring insulin treatment
Patients with congestive heart failure that requires treatment
History of heart attack or stroke, or within the last 12
months had by-pass surgery or angioplasty
History of severe kidney, liver, or muscular disease
For additional information about this trial, contact:
Sheryl Grant, Study Coordinator
Jacksonville Center for Clinical Research
4085 University Blvd S, Suite 1
Jacksonville, FL 32216
Telephone: 904-730-0101
Fax: 904-730-0121
Summary: A study to evaluate the effects of two FDA approved
medications for high blood pressure in patients with kidney disease
This study evaluates the effects of two FDA approved medications
for high blood pressure in patients with renal insufficiency to
examine the safety and effectiveness of the two medications on
the kidneys.
Participants in the 8-week study will be required to attend eight
office visits during that time. However, participants may have
to return more often to complete or repeat procedures. Each visit
should not take more than an hour.
Clinical Trial Eligibility Criteria:
History or a new diagnosis of renal impairment
History or a new diagnosis of hypertension or newly diagnosis
Contact:
Rolanda J. Flynn, Project Coordinator
Department of Preventive Medicine at Rush
University Medical Center
1700 West VanBuren, Suite 470
Chicago, IL 60612
Telephone: 312-563-2242
Email: rflynn@rush.edu
Summary: High Blood Pressure
Hows your blood pressure? The time it takes to get your
blood pressure checked might be the few minutes that could save
your life.
Clinical Research Associates, Inc. is recruiting volunteers, ages
18-80, who have been diagnosed with high blood pressure to participate
in a research study to determine the efficacy and safety of an
investigational treatment for hypertension. Participants will
receive study medications and exams, lab work, and compensation
for participation.
For additional information about this study or to enroll, contact:
Recruiting Coordinator
Clinical Research Associates, Inc.
2222 State Street, Suites B & D
Nashville, TN 37203
Telephone: 615-329-2222
To find clinical trials in your area, go to: http://www.centerwatch.com/search.asp
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