Overview
A 52 Week Study to Evaluate the Effects of Losartan With or Without HCTZ on Plasma Glucose, Metabolic Parameters, Blood Pressure in Hypertensive Patients With Metabolic Syndrome (0954A-331)
Status:
Completed
Completed
Trial end date:
2008-01-01
2008-01-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
To determine if a one year treatment Losartan with or without HCTZ at different dosages have an effect on metabolic parameters in patients with hypertension and the metabolic syndrome.Phase:
Phase 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Merck Sharp & Dohme Corp.Treatments:
Hydrochlorothiazide
Losartan
Criteria
Inclusion Criteria:- An Adult Patient (At Least 18 Years Of Age) With A Clinical Identification Of The
Metabolic Syndrome Using The IDF Definition:
- abdominal (central) obesity as defined by the waist circumference in men of > 102
cm and women of > 88 cm or a BMI equal or greater than 30 kg/m2
and untreated hypertension with bp equal or greater than 140/90 mm Hg but bp < 180/110 mm
Hg
or a patient receiving one or two antihypertensive agent(s) (diuretics, ace inhibitors,
angiotensin ii receptor blockers, calcium channel blockers and beta-blockers will need to
be discontinued) and whose blood pressure is not controlled:
- bp equal or greater than 140/90 mm Hg but equal or less than 160/100 mm Hg
or a patient whose hypertension is controlled (< 140/90 mm hg) with a single
anti-hypertensive agent (diuretics, ace inhibitors, and angiotensin II receptor blockers,
calcium channel blockers and beta-blockers will need to be discontinued) but who is
unsatisfied or experiencing side effects warranting a discontinuation of the previous
treatment and at one of the following:
- Fasting plasma glucose equal or greater than 5.6 mmol/L and < 7.0 mmol/L
- Triglycerides > 1.7 mmol/L or specific treatment for this lipid abnormality
- HDL-c in men < 0.9 mmol/L and in women < 1.1 mmol/L or specific treatment for this
lipid abnormality
Exclusion Criteria:
- A Patient With A Diagnosis Of Type II Diabetes Defined As Fasting Blood Glucose Level
Equal Or Greater Than 7.0 Mmol/L Or A 2hpg In A 75-G OGTT Equal Or Greater Than 11.1
Mol/L Or Using Any Anti-Hyperglycemic Agents
- Known Secondary Hypertension Of Any Aetiology (E.G., Uncorrected Renal Artery
Stenosis, Malignant Hypertension, Or Hypertensive Encephalopathy)
- Patient Intolerant To Any Component Of Losartan 50 Mg / Losartan 100 Mg / Losartan 100
Mg + Hctz 12.5 Mg / Losartan 100 Mg + Hctz 25 Mg Or With A Documented History Of
Angioedema
- Patient With Confirmed Clinically Significant Renal Or Hepatic Dysfunction And/Or
Electrolyte Imbalance On The Basis Of The Case History Or A Recent Laboratory Test
(Serum Creatinine > 130 Mmol/L Or Creatinine Clearance < 45 Ml/Min, Ast > 2 Times
Above The Normal Range, Alt > 2 Times Above The Normal Range, Serum Potassium < 3.5 Or
> 5.5 Meq/L)
- Patient With Symptomatic Heart Failure (Classes 3 And 4)
- Patient With A Prior Myocardial Infarction Or Stroke Within The Last 6 Months
- Patient Who Has Undergone Percutaneous Coronary Angioplasty Or Coronary Artery Bypass
Within The Last 3 Months
- Pregnant Woman Or A Woman Of Childbearing Potential