NCT Number: NCT02235415
Observation of the Efficacy and Tolerance of Motens® (Lacidipine) in Patients With Essential Hypertension
Study of the efficacy and tolerance of Motens® (lacidipine) in patients with essential hypertension. To obtain information on the dosage used in practice and the tolerance at the start of treatment (12 weeks)
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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
Non-hospitalised patients of both sexes aged 18 years or more with essential hypertension requiring treatment according to the recommendations of the German League for Hypertension
Exclusion criteria
Patients who had the contraindications listed in the product information (the case report file contained a copy of the product information)
Treatment and study plan
Primary outcomes
-
Assessment of efficacy by the investigator on a 4-point verbal rating scale based on changes in blood pressure
Time frame: Up to 12 weeks after start of drug administration
-
Assessment of tolerability by investigator on a 4-point verbal rating scale
Time frame: Up to 12 weeks after start of drug administration
-
Number of patients with adverse events
Time frame: Up to 12 weeks after start of drug administration
Sponsors and collaborators
Lead sponsor
Boehringer Ingelheim
Industry
Registry information
Official study title
Observation of the Efficacy and Tolerance of Motens® (Lacidipine) in Patients With Essential Hypertension, Under Normal Conditions Compared With an Open Clinical Trial
Important dates
- Study start
- 1998
- Primary completion
- 1999
- First posted
- Sep 10, 2014
- Registry last updated
- Sep 10, 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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