NCT Number: NCT00140959
Losartan and HCTZ and Amlodipine vs Atenolol and Amlodipine (0954A-309)(COMPLETED)
A study to evaluate the effects of combination losartan versus combination atenolol in patients with ambulatory systolic hypertension.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 4
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Males or females at least 18 years of age who have ambulatory systolic hypertension.
Treatment and study plan
Comparator: losartan, HCTZ, amlodipine, atenolol/Duration of Treatment: 18 weeks
DrugPrimary outcomes
-
Mean daytime ambulatory systolic blood pressure
Secondary outcomes
-
Ambulatory BP
-
Pulse pressure
-
Trough sitting BP
-
Percentage of patients who reach goal ambulatory systolic BP
Sponsors and collaborators
Lead sponsor
Organon and Co
Industry
Registry information
Official study title
Antihypertensive Effects of a Fixed-dose Combination of Losartan and Hydrochlorothiazide Plus Amlodipine Versus a Hydrochlorothiazide and Atenolol Combination Plus Amlodipine in Subjects With Ambulatory Systolic Hypertension.
Important dates
- Study start
- 2003
- Primary completion
- 2004
- Study completion
- 2004
- First posted
- Sep 1, 2005
- Registry last updated
- Aug 15, 2024
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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