Trials / Completed
CompletedNCT00509470
Evaluation of Effect of Combination With Telmisartan and Hydrochlorothiazide in Hypertensives Uncontrolled on Amlodipine
ONgoing Evaluation of Depressor Effect And Safety of Combination Therapy With Telmisartan and Low-dose Hydrochlorothiazide in Patients With Hypertension Uncontrolled on Amlodipine Treatment
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 75 (actual)
- Sponsor
- Tokyo University · Academic / Other
- Sex
- All
- Age
- 40 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to compare depressor effect and safety between combination therapy with telmisartan plus low-dose hydrochlorothiazide and amlodipine in hypertensive patients.
Detailed description
In hypertensive patients whose blood pressure (BP) does not reach less than 140/90 mmHg with 5mg/day of amlodipine are divided the following two groups and BP response, laboratory data, and adverse effects are compared. Group 1: 12 week combination therapy with telmisartan plus low-dose hydrochlorothiazide. Group 2: Amlodipine is continuously administered.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | telmisartan plus hydrochlorothiazide | Combination therapy with telmisartan (40 mg/day) plus hydrochlorothiazide (12.5 mg/day): If blood pressure is not reach to lower than 140/90 mmHg, dose of telmisartan can be increased to 80 mg/day |
| DEVICE | Amlodipine |
Timeline
- Start date
- 2007-07-01
- Primary completion
- 2012-06-01
- Completion
- 2012-10-01
- First posted
- 2007-07-31
- Last updated
- 2016-10-18
Locations
1 site across 1 country: Japan
Source: ClinicalTrials.gov record NCT00509470. Inclusion in this directory is not an endorsement.