- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01138423
Treatment of Adiposity Related hypErTension (TARGET) (TARGET)
A Randomized, Placebo-controlled, Double Blind, 4-period, Cross-over Trial, to Study the Effects of Aliskiren, Hydrochlorothiazide and Moxonidine on Endothelial Dysfunction in Obesity Related Hypertension
High blood pressure (hypertension) is an important cause of myocardial infarction and stroke. High blood pressure often occurs in people who are overweight. These people frequently also have abnormal fat and sugar metabolism. The combination of these problems is called the 'metabolic syndrome'.
People with hypertension and obesity currently receive the same drug therapy as people with hypertension, but without obesity. Different classes of drugs are thought to be equally effective in lowering blood pressure.
Next to lowering blood pressure, hypertension treatment can have additional effects, like changes in blood vessel function (the ability to dilate and constrict) or changes is the metabolism of sugar and fat. Particularly in patients with the metabolic syndrome, these additional effects are thought to be of great importance, because they can influence the risk for cardiovascular diseases.
The blood pressure lowering mechanism differs between classes of blood pressure lowering medication. The purpose of this study is to compare the effects of three types of blood pressure lowering medication belonging to different classes. The main outcomes of interest will be blood vessel function (the ability to dilate and constrict) and blood pressure. Moreover, the effect of treatment on additional outcomes, like metabolism of sugar and fat, will be studied.
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Phase 4
Contacts and Locations
Study Locations
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-
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Utrecht, Netherlands, 3508 GA
- UMC Utrecht
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion criteria:
- Patient is a male or post menopausal female, 30-70 years of age on the day of signing informed consent. Post menopausal status is assumed if a woman has not experienced a menstrual bleed for a minimum of 12 months, assuming that she still has a uterus, and is not pregnant or lactating. In women without a uterus, menopause or postmenopause is defined by a very high FSH level.
- All patients should fulfil the diagnostic criterion of abdominal adiposity: waist circumference > 102 cm (men) or > 88 cm (women). The waist circumference is measured halfway between the lower rib and iliac crest in standing position.
- All patients should fulfil the diagnostic criterium for hypertension: systolic blood pressure >/= 130 mmHg and/or diastolic blood pressure >/= 85 mmHg during both visits. Blood pressure is assessed by office readings in accordance with current guidelines for hypertension diagnosis. The patient needs to be seated some minutes before and during the measurement. The cuff size should be adjusted to the patients' arm circumference and needs to be on the same height level as the patients' sternum during the measurements. Blood pressure is determined to a 2 mmHg accuracy-level. Blood pressure is measured on both arms during the first visit. In both measurements differ more than 10 mmHg, the highest value is taken. After at least 15 seconds, the measurement is repeated during the same visit. The highest mean of the two measurements on the same arm is considered as the actual blood pressure value.
- Patients should fulfil one or more of the following criteria to meet the definition of the metabolic syndrome: 1)Hypertriglyceridemia (serum triglycerides > 1.7 mmol/L); 2) Low High-density lipoprotein (HDL)-cholesterol (serum HDL-cholesterol < 1.04 mmol/L (men) or < 1.29 mmol/L (women)); 3)High fasting glucose (fasting serum glucose > 5.6 mmol/L).
- Patient understands the study procedures, alternative treatments available, and risks involved with the study and voluntarily agrees to participate by giving written informed consent.
Exclusion criteria:
- Systolic blood pressure > 180 mmHg and/or diastolic blood pressure > 110 mmHg during one or more screening measurements.
- Body Mass Index (BMI) > 35 kg/m2
- Current smoking or smoking during the previous 3 months
- Use of "recreational" or illicit drugs
- Recent history (within the last year) of alcohol abuse or dependence.
- History of hypersensitivity reactions or intolerance to any (components of) medication used in this trial.
- Current / recent participation (within 30 days of signing informed consent) in a study with an investigational compound or device.
- Laboratory values as follows: Hemoglobin (Hb) < 8,6 mmol/L (men) or < 7.4 mmol/L (women); TSH <0.3 mcIU/mL or > 5.0 mcIU/mL; Potassium < 3,8 mmol/L or > 5,0 mmol/L; Sodium < 136 mmol/L or > 146 mmol/L; MDRD < 60 mL/min/1,73m2
- Medical conditions as follows: Resistant hypertension (blood pressure above target level, despite 3 antihypertensives, including a diuretic); Secondary hypertension; Congestive Heart Failure; Atherosclerotic vascular disease (As per NCEP ATP III and AHA/ACC Guidelines); Cardiac arrhythmia's, for example bradycardia, atrial fibrillation, sick-sinus syndrome, sinoatrial block, atrioventricular block or any other arrhythmia; Obstructive sleep apnea syndrome (OSAS) or a score of 10 or higher on the Epworth Sleepiness Scale questionnaire; Serious liver function disorders (Child-Pugh-Class C); COPD (GOLD classification of severity 2 or higher); Celiac disease or other significant intestinal malabsorption; Malignancy ≤ 5 years prior to signing informed consent, except for adequately treated basal or squamous cell skin cancer or in situ cervical cancer; Mental instability or major psychiatric illness; Polyneuropathy or clinical suspicion for autonomic nervous system dysfunction; Any diseases that would limit or complicate study evaluation or participation; Any diseases or screening abnormalities that call for treatment that can not be postponed until after the study period without causing harm.
- Any concomitant medication, particularly antihypertensive co-medication, glucose lowering medication, lipid lowering drugs, systemic corticosteroids, birth control pills and vitamin C or E supplements, but also any other kinds of drugs, including over the counter medication. Exceptions can be made for the following categories of drugs: paracetamol; proton-pump inhibitors; topical creams and unguents that do not lead to uptake of any of the active components into the circulation (in case of steroid creams: class II or lower); inhalation medication, nasal sprays and eye drops that do not lead to uptake of any of the active components into the circulation.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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Placebo Comparator: Placebo
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Once daily treatment with placebo capsules for 8-weeks, according to the following regiment: once daily (morning time) 1 capsule during the first 2 weeks, followed by once daily (morning time) 2 capsules during the remaining 6 weeks.
Coincidental intake of grapefruit(juice) should be avoided.
This treatment interval is followed by a one-week tapering period: 1 tablet on day 1, 2, 3, 4, 5 and 7.
Once daily treatment with placebo tablets for 8-weeks, according to the following regiment: once daily (morning time) 1 tablet during the first 2 weeks, followed by once daily (morning time) 2 tablets during the remaining 6 weeks.
Coincidental intake of grapefruit(juice) should be avoided.
This treatment interval is followed by a one-week tapering period: 1 tablet on day 1, 2, 3, 4, 5 and 7.
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Experimental: Moxonidine
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Once daily treatment with moxonidine for 8-weeks, according to the following regiment: once daily (morning time) 0.2 mg during the first 2 weeks, followed by once daily (morning time) 0.4 mg during the remaining 6 weeks.
Coincidental intake of grapefruit(juice) should be avoided.
This treatment interval is followed by a one-week tapering period: 0.2 mg on day 1, 2, 3, 4, 5 and 7.
Other Names:
Once daily treatment with placebo tablets for 8-weeks, according to the following regiment: once daily (morning time) 1 tablet during the first 2 weeks, followed by once daily (morning time) 2 tablets during the remaining 6 weeks.
Coincidental intake of grapefruit(juice) should be avoided.
This treatment interval is followed by a one-week tapering period: 1 tablet on day 1, 2, 3, 4, 5 and 7.
|
Experimental: Aliskiren
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Once daily treatment with aliskiren for 8-weeks, according to the following regiment: once daily (morning time) 150 mg during the first 2 weeks, followed by once daily (morning time) 300 mg during the remaining 6 weeks.
Coincidental intake of grapefruit(juice) should be avoided.
This treatment interval is followed by a one-week tapering period: 150 mg on day 1, 2, 3, 4, 5 and 7.
Other Names:
Once daily treatment with placebo capsules for 8-weeks, according to the following regiment: once daily (morning time) 1 capsule during the first 2 weeks, followed by once daily (morning time) 2 capsules during the remaining 6 weeks.
Coincidental intake of grapefruit(juice) should be avoided.
This treatment interval is followed by a one-week tapering period: 1 tablet on day 1, 2, 3, 4, 5 and 7.
|
Experimental: Hydrochlorothiazide
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Once daily treatment with placebo tablets for 8-weeks, according to the following regiment: once daily (morning time) 1 tablet during the first 2 weeks, followed by once daily (morning time) 2 tablets during the remaining 6 weeks.
Coincidental intake of grapefruit(juice) should be avoided.
This treatment interval is followed by a one-week tapering period: 1 tablet on day 1, 2, 3, 4, 5 and 7.
Once daily treatment with hydrochlorothiazide for 8-weeks, according to the following regiment: once daily (morning time) 12.5 mg during the first 2 weeks, followed by once daily (morning time) 25 mg during the remaining 6 weeks.
Coincidental intake of grapefruit(juice) should be avoided.
This treatment interval is followed by a one-week tapering period: 12.5 mg on day 1, 2, 3, 4, 5 and 7.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Endothelial function assessed by Flow Mediated Dilation (FMD)
Time Frame: After 8 weeks treatment
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After 8 weeks treatment
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Mean 24-hour systolic/diastolic blood pressure Mean day- and night time systolic/diastolic blood pressure
Time Frame: After 8 weeks treatment
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After 8 weeks treatment
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Central Blood pressure (estimated with pulse wave analysis)
Time Frame: After 8 weeks treatment
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After 8 weeks treatment
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Renin-Angiotensin System (RAS) hormone concentrations
Time Frame: After 8 weeks treatment
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After 8 weeks treatment
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Sympathetic nervous system activity, assessed by Muscle Sympathetic Nerve Activity (MSNA) and Heart Rate Variability (HRV)
Time Frame: After 8 weeks treatment
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After 8 weeks treatment
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Markers of oxidative stress (concentrations of F2-isoprostanes in urine and oxLDL in plasma)
Time Frame: After 8 weeks treatment
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After 8 weeks treatment
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Markers of inflammation (hs-CRP in plasma)
Time Frame: After 8 weeks treatment
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After 8 weeks treatment
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Fractional sodium excretion
Time Frame: After 8 weeks treatment
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After 8 weeks treatment
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Arterial stiffness (assessed by pulse wave velocity and the pulse wave analysis augmentation index)
Time Frame: After 8 weeks treatment
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After 8 weeks treatment
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Adipose tissue function (serum concentrations of adipokines)
Time Frame: After 8 weeks treatment
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After 8 weeks treatment
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Lipid metabolism (serum lipid concentrations)
Time Frame: After 8 weeks treatment
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After 8 weeks treatment
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Insulin sensitivity, expressed by homeostatic model assessment (HOMA)
Time Frame: After 8 weeks treatment
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After 8 weeks treatment
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Chair: F.L.J. Visseren, Professor (MD PhD), UMC Utrecht
- Principal Investigator: W. Spiering, MD PhD, UMC Utrecht
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Cardiovascular Diseases
- Vascular Diseases
- Glucose Metabolism Disorders
- Metabolic Diseases
- Overnutrition
- Nutrition Disorders
- Overweight
- Body Weight
- Insulin Resistance
- Hyperinsulinism
- Hypertension
- Obesity
- Metabolic Syndrome
- Obesity, Abdominal
- Physiological Effects of Drugs
- Molecular Mechanisms of Pharmacological Action
- Antihypertensive Agents
- Natriuretic Agents
- Membrane Transport Modulators
- Diuretics
- Sodium Chloride Symporter Inhibitors
- Hydrochlorothiazide
- Moxonidine
Other Study ID Numbers
- UMCU-Vasc-14A
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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