NCT Number: NCT02262611
Post Marketing Surveillance Study in Rehabilitation Clinics (Cardio, Nephro, Diabetes, Pulmo)
Study to obtain long-term data on effects, safety and tolerability in routine medical practice and to investigate the potential of telmisartan to prevent secondary organ damage
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Observational
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Adult patients of both gender aged >=18 admitted to a hospital due to insufficiently controlled essential hypertension.
No additional selection criteria have to be considered. Treatment was at the discretion of the physician following the summary of product information for Micardis® and MicardisPlus®
Exclusion criteria
- not applicable
Treatment and study plan
MicardisPlus®
DrugPrimary outcomes
-
Number of patients with adverse events
Time frame: up to 1 year
-
Number of patients with abnormal changes in laboratory parameters
Time frame: up to 1 year
-
Number of patients with clinically significant changes in vital signs
Time frame: up to 1 year
-
Change in systolic blood pressure
Time frame: up to 1 year
-
Change in diastolic blood pressure
Time frame: up to 1 year
Secondary outcomes
-
Global assessment of efficacy by investigator on a 4-point scale
Time frame: 2 weeks, after 1 year
-
Global assessment of tolerability by investigator on a 4-point scale
Time frame: 2 weeks, after 1 year
Sponsors and collaborators
Lead sponsor
Boehringer Ingelheim
Industry
Registry information
Important dates
- Study start
- 2003
- Primary completion
- 2005
- First posted
- Oct 13, 2014
- Registry last updated
- Oct 13, 2014
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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