Clinical Trials Directory

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

TypeNameDescription
DRUGTelmisartan/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.

Effects of Telmisartan/Hydrochlorothiazide Treatment in Hypertensive Patients Under Real-life Setting (NCT01392534) · Clinical Trials Directory