Full Text View  
  Tabular View  
  Contacts and Locations  
  No Study Results Posted  
  Related Studies  
Ramipril and Hydrochlorothiazide Alone and in Combination for the Treatment of Essential Hypertension
This study has been completed.
Sponsored by: King Pharmaceuticals Research and Development
Information provided by: King Pharmaceuticals Research and Development
ClinicalTrials.gov Identifier: NCT00355589
  Purpose

The purpose of this study is to determine if there is greater blood pressure reduction using ramipril or hydrochlorothiazide alone or ramipril and hydrochlorothiazide together.


Condition Intervention Phase
Hypertension
Blood Pressure, High
Drug: Ramipril and hydrochlorothiazide
Phase III

MedlinePlus related topics: High Blood Pressure
Drug Information available for: Hydrochlorothiazide Ramipril
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Safety/Efficacy Study
Official Title: A Randomized, Double-Blind, Multicenter, Parallel Study Evaluating the Efficacy and Safety of a Combination of Ramipril Plus Hydrochlorothiazide Versus the Component Monotherapies in Subjects With Essential Hypertension

Further study details as provided by King Pharmaceuticals Research and Development:

Primary Outcome Measures:
  • Compare the effects on sitting diastolic blood pressure of two antihypertensive drugs in combination against each antihypertensive alone after an eight week treatment period.

Secondary Outcome Measures:
  • Compare the effect on sitting diastolic blood pressure of two antihypertensive drugs in combination taken once daily against one antihypertensive drug taken twice daily.
  • Compare the effect on sitting diastolic blood pressure of a dose of an antihypertensive drug taken once daily against half of the same dose taken twice daily.
  • Compare the effect on the sitting and standing blood pressure among all treatment groups.
  • Compare the safety of each medication regimen stated above.
  • Compare the effect on mean 24-hour diastolic blood pressure (ABPM) of the medication regimens stated above.

  Eligibility

Ages Eligible for Study:   18 Years to 80 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Previously diagnosed, or newly diagnosed essential hypertension. Blood pressure must be within a minimum and maximum range prior to drug treatment.

Exclusion Criteria:

  • Inability to discontinue all prior antihypertensive medications
  • Heart failure
  • History of stroke, myocardial infarction, or chest pain within 3 years, or an abnormal heart rhythm
  • Liver or kidney disease
  • Certain drugs used to treat other conditions like an enlarged prostate gland, or arthritis
  • Allergy or reactions to certain medications used to treat high blood pressure

Other protocol-defined inclusion and exclusion criteria apply.

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00355589

  Show 60 Study Locations
Sponsors and Collaborators
King Pharmaceuticals Research and Development
  More Information

Publications indexed to this study:
Study ID Numbers: K749-06-3001
Study First Received: July 20, 2006
Last Updated: November 12, 2007
ClinicalTrials.gov Identifier: NCT00355589  
Health Authority: United States: Food and Drug Administration

Keywords provided by King Pharmaceuticals Research and Development:
Hypertension
High Blood Pressure
Diuretic
Angiotensin converting enzyme inhibitor
Ambulatory blood pressure monitoring

Study placed in the following topic categories:
Vascular Diseases
Essential hypertension
Hydrochlorothiazide
Ramipril
Hypertension

Additional relevant MeSH terms:
Molecular Mechanisms of Pharmacological Action
Diuretics
Physiological Effects of Drugs
Sodium Chloride Symporter Inhibitors
Enzyme Inhibitors
Cardiovascular Agents
Antihypertensive Agents
Pharmacologic Actions
Protease Inhibitors
Membrane Transport Modulators
Natriuretic Agents
Therapeutic Uses
Angiotensin-Converting Enzyme Inhibitors
Cardiovascular Diseases

ClinicalTrials.gov processed this record on January 14, 2009