NCT Number: NCT02242370
Effectiveness of MICARDIS® (Telmisartan) on Blood Pressure Control and Quality of Live in Patients With Essential Hypertension
Study to assess the effect of Telmisartan on diastolic and systolic blood pressure and to establish the effect on patient's quality of life scores.
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Notify MeKey information
Conditions
Age range
20 year–93 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 4
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Patients with Stage I essential Hypertension (diastolic blood pressure 90-99 mmHg, and/or systolic blood pressure 140-159 mmHg)
- Signed informed consent form
Exclusion criteria
- Females of childbearing potential
Treatment and study plan
High dose of telmisartan
DrugPrimary outcomes
-
Change in diastolic blood pressure
Time frame: Pre-dose, up to 6 weeks after start of treatment
-
Change in systolic blood pressure
Time frame: Pre-dose, up to 6 weeks after start of treatment
-
Changes from baseline in the quality of life (QOL) scores by patient self-assessment
Time frame: Pre-dose, 6 weeks after start of treatment
Secondary outcomes
-
Assessment of blood pressure control rate
Time frame: Up to 6 weeks after start of treatment
-
Assessment of systolic blood pressure response rate
Time frame: Up to 6 weeks after start of treatment
-
Assessment of diastolic blood pressure response rate
Time frame: Up to 6 weeks after start of treatment
-
Change from baseline in pulse pressure
Time frame: Pre-dose, up to 6 weeks after start of treatment
-
Number of patients with adverse events
Time frame: Up to 6 weeks
Sponsors and collaborators
Lead sponsor
Boehringer Ingelheim
Industry
Registry information
Official study title
An Open-label Evaluation of the Effectiveness of MICARDIS® (Telmisartan) on Blood Pressure Control and Quality of Life in Patients With Essential Hypertension The MICARDIS COMMUNITY ACCESS TRIAL (MicCAT)
Acronym: MicCAT
Important dates
- Study start
- 1999
- Primary completion
- 2000
- First posted
- Sep 17, 2014
- Registry last updated
- Sep 17, 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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