Use of the Combination of Olmesartan and Hydrochlorothiazide in Essential Hypertension - Full Text View

Sponsor:	Daiichi Sankyo Inc.
Collaborator:	Daiichi Sankyo Europe, GmbH
Information provided by:	Daiichi Sankyo Inc.
ClinicalTrials.gov Identifier:	NCT00430508

Purpose

The study will evaluate the blood pressure lowering effects of two different dosages of the combination of olmesartan and hydrochlorothiazide in patients with moderate or severe high blood pressure.

Condition	Intervention	Phase
Essential Hypertension	Drug: olmesartan medoxomil (OM)/hydrochlorothiazide (HCTZ) tablets and placebo Drug: olmesartan medoxomil (OM)/hydrochlorothiazide (HCTZ) tablets Drug: olmesartan medoxomil/hydrochlorothiazide tablets	Phase III

Study Type:	Interventional
Study Design:	Treatment, Randomized, Double Blind (Subject, Investigator), Active Control, Parallel Assignment, Safety/Efficacy Study
Official Title:	Efficacy and Safety of Hydrochlorothiazide (HCTZ) Used as Add-on Therapy in Moderately to Severely Hypertensive Patients Not Adequately Controlled by Olmesartan Medoxomil (OM) 40 mg Monotherapy

Resource links provided by NLM:

MedlinePlus related topics: High Blood Pressure

Drug Information available for: Hydrochlorothiazide Olmesartan Olmesartan medoxomil

U.S. FDA Resources

Further study details as provided by Daiichi Sankyo Inc.:

Primary Outcome Measures:

Change in Mean Trough Sitting Diastolic Blood Pressure From Week 8(Baseline) to Week 16 [ Time Frame: 8 weeks, change = week 16 - week 8 ] [ Designated as safety issue: No ]

Secondary Outcome Measures:

Change in Mean Trough Sitting Diastolic Blood Pressure From Week 8(Baseline) to Week 12. [ Time Frame: 4 weeks, change = week 12 - week 8 ] [ Designated as safety issue: No ]
Change in Mean Trough Sitting Systolic Blood Pressure From Week 8(Baseline) to Week 16. [ Time Frame: 8 weeks, change = week 16 - week 8 ] [ Designated as safety issue: No ]
Change in Mean Trough Sitting Systolic Blood Pressure From Week 8(Baseline) to Week 12. [ Time Frame: 4 weeks, change = week 12 - week 8 ] [ Designated as safety issue: No ]
Number of Patients Achieving Target Blood Pressure at Week 16 [ Time Frame: 8 weeks ] [ Designated as safety issue: No ]
Change in Mean 24-Hour Ambulatory Blood Pressure Monitoring Diastolic Blood Pressure From Week 8(Baseline) to Week 16. [ Time Frame: 8 weeks, change = week 16 - week 8 ] [ Designated as safety issue: No ]
Change in Mean Daytime Ambulatory Blood Pressure Monitoring Diastolic Blood Pressure From Week 8(Baseline) to Week 16. [ Time Frame: 8 weeks, change = week 16 - week 8 ] [ Designated as safety issue: No ]
Change in Mean Night-Time Ambulatory Blood Pressure Monitoring Diastolic Blood Pressure From Week 8(Baseline) to Week 16. [ Time Frame: 8 weeks, change = week 16 - week 8 ] [ Designated as safety issue: No ]

Enrollment:	972
Study Start Date:	February 2007
Study Completion Date:	May 2008
Primary Completion Date:	March 2008 (Final data collection date for primary outcome measure)

Arms	Assigned Interventions
4: Experimental olmesartan medoxomil (OM) /hydrochlorothiazide (HCTZ) Tablet 40mg/0mg + 20mg/12.5mg matching placebo tablet once daily for 8 weeks	Drug: olmesartan medoxomil (OM)/hydrochlorothiazide (HCTZ) tablets and placebo olmesartan medoxomil (OM)/hydrochlorothiazide (HCTZ) Tablet 40mg/0mg + 20mg/12.5mg matching placebo tablet once daily for 8 week
1: Experimental olmesartan medoxomil (OM) /hydrochlorothiazide (HCTZ) tablets 40mg/25mg + 20mg/12.5mg matching placebo tablet once daily for 8 weeks	Drug: olmesartan medoxomil/hydrochlorothiazide tablets olmesartan medoxomil (OM)/hydrochlorothiazide (HCTZ) tablets 40mg/25mg + 20mg/12.5mg matching placebo tablet once daily for 8 weeks
3: Experimental olmesartan medoxomil (OM)/hydrochlorothiazide (HCTZ) tablets 20mg/12.5mg + 40mg/0mg matching placebo tablet once daily for 8 weeks	Drug: olmesartan medoxomil/hydrochlorothiazide tablets olmesartan medoxomil (OM)/hydrochlorothiazide (HCTZ) tablets 20mg/12.5mg + 40mg/0mg matching placebo tablet once daily for 8 weeks
2: Experimental olmesartan medoxomil (OM)/hydrochlorothiazide (HCTZ) tablets 40mg/12.5mg + 20mg/12.5mg matching placebo tablet once daily for 8 weeks	Drug: olmesartan medoxomil (OM)/hydrochlorothiazide (HCTZ) tablets olmesartan medoxomil (OM)/hydrochlorothiazide (HCTZ) tablets 40mg/12.5mg + 20mg/12.5mg matching placebo tablet once daily for 8 weeks

Eligibility

Ages Eligible for Study:	18 Years and older
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

Male or female Europeans aged 18 years or older with moderate to severe hypertension (HTN)

Exclusion Criteria:

Female patients of childbearing potential pregnant, lactating or planning to become pregnant during the trial period.
Patients with serious disorders which may limit the ability to evaluate the efficacy or safety of the study medication, including cerebrovascular, cardiovascular, renal, respiratory, hepatic, gastrointestinal, endocrine or metabolic, haematological or oncological, neurological and psychiatric diseases.
Patients having a history of the following within the last six months:
- myocardial infarction,
- unstable angina pectoris,
- percutaneous coronary intervention,
- severe heart failure,
- hypertensive encephalopathy,
- cerebrovascular accident (stroke) or
- transient ischaemic attack.
Patients with clinically significant abnormal laboratory values at screening.
Patients with secondary HTN.

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00430508

Show 55 Study Locations

Sponsors and Collaborators

Daiichi Sankyo Inc.

Daiichi Sankyo Europe, GmbH

Investigators

Study Chair:

Professor Lars Christian Rump, M.D.

University of Ruhr-Bochum

More Information

No publications provided

Responsible Party:	Daichi Sankyo Europe, GmbH ( Bettina Ammentorp )
Study ID Numbers:	CS866CM-B-E301
Study First Received:	February 1, 2007
Results First Received:	February 9, 2009
Last Updated:	June 17, 2009
ClinicalTrials.gov Identifier:	NCT00430508 History of Changes
Health Authority:	EU: EMEA; Germany: Bundesministerium fur; Spain: Ministry of Health; Italy: Ministry of Health; France: Afssaps - French Health Products Safety Agency; Bulgaria: Bulgarian Drug Agency; Ukraine: Ministry of Health; Czech Republic: State Institute for Drug Control; Poland: Office for Registration of Medicinal Products, Medical Devices and Biocidal Products

Keywords provided by Daiichi Sankyo Inc.:

Moderate-to-Severe Hypertension
Essential Hypertension
Combination Therapy
Fixed-Combination Dose

Additional relevant MeSH terms:

Molecular Mechanisms of Pharmacological Action
Diuretics
Physiological Effects of Drugs
Sodium Chloride Symporter Inhibitors
Vascular Diseases
Olmesartan medoxomil
Cardiovascular Agents
Antihypertensive Agents

Hydrochlorothiazide
Pharmacologic Actions
Angiotensin II Type 1 Receptor Blockers
Membrane Transport Modulators
Natriuretic Agents
Therapeutic Uses
Cardiovascular Diseases
Hypertension

ClinicalTrials.gov processed this record on February 08, 2010