Trials / Completed
CompletedNCT01392534
Effects of Telmisartan/Hydrochlorothiazide Treatment in Hypertensive Patients Under Real-life Setting
Evaluation of the Real-life Efficacy and Safety of a Fixed-dose Telmisartan/Hydrochlorothiazide, Including Its Effect on Plasma Potassium and on Glucose and Lipid Metabolism Parameters in Patients With Essential Arterial Hypertension
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 1,586 (actual)
- Sponsor
- Bayer · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
One of the most common adverse effects resulting from the therapy with thiazides, thiazide-like diuretics and loop diuretics is increased potassium secretion. Disregulation of plasma potassium may be a life-threatening condition due to increased risk of arrythmias. Moreover, it has been postulated that decrease in plasma potassium level may negatively affect glucose metabolism resulting in the increased risk of new-onset type 2 diabetes.The main goal of this study is to assess the efficacy and safety of telmisartan/hydrochlorothiazide in a broad population of hypertensive patients, including the effects of the therapy on plasma potassium level and also on selected parameters of glucose and lipid metabolism.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Telmisartan/hydrochlorothiazide (Pritor Plus, BAY98-7103) | Patients treated with telmisartan/hydrochlorothiazide tablets under the real-life setting. Dosing regimen customised to the needs of each participating patient according to the investigators assessment |
Timeline
- Start date
- 2010-07-01
- Primary completion
- 2010-12-01
- Completion
- 2010-12-01
- First posted
- 2011-07-12
- Last updated
- 2012-07-04
Locations
1 site across 1 country: Poland
Source: ClinicalTrials.gov record NCT01392534. Inclusion in this directory is not an endorsement.