Clinical Trials Directory

Trials / Completed

CompletedNCT02756819

International Multicenter, Observational, Non-Interventional Prospective Study of Azilsartan Medoxomil in Participants With Arterial Hypertension Who Are Overweight or Obese in the Russian Federation and The Republic of Kazakhstan

International Multicentre, Observational, Non-Interventional Prospective Study of Azilsartan Medoxomil in Patients With Arterial Hypertension Who Are Overweight or Obese in the Russian Federation and The Republic of Kazakhstan

Status
Completed
Phase
Study type
Observational
Enrollment
1,945 (actual)
Sponsor
Takeda · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to estimate antihypertensive effect of azilsartan medoxomil (Edarbi®) therapy on blood pressure in participants with overweight or obesity in routine clinical practice of hypertension (HTN) treatment in the Russian Federation and in the Republic of Kazakhstan..

Detailed description

The drug being tested in this study is called azilsartan medoxomil (Edarbi®). Azilsartan medoxomil is being tested to treat people who have hypertension. This study looks at the clinic systolic and diastolic blood pressure (SBP, DBP) in obese participants who were prescribed azilsartan medoxomil by physicians. The study enrolled 1945 patients. All participants were asked to take azilsartan medoxomil as prescribed by their physician according to local SmPC. This multi-center trial was conducted in the Russian Federation and the Republic of Kazakhstan. The overall duration of study for observation was approximately 6 months. Participants made multiple visits to the clinics as assigned by each physician according to their routine practice, in every 3 months.

Conditions

Interventions

TypeNameDescription
DRUGAzilsartan MedoxomilAzilsartan medoxomil tablets

Timeline

Start date
2016-07-18
Primary completion
2018-05-08
Completion
2018-05-08
First posted
2016-04-29
Last updated
2019-11-20
Results posted
2019-11-20

Locations

66 sites across 2 countries: Kazakhstan, Russia

Regulatory

Source: ClinicalTrials.gov record NCT02756819. Inclusion in this directory is not an endorsement.