Observation of Therapy With Micardis® (Telmisartan) in Patients With Essential Hypertension in Hospitals
1 other identifier
observational
2,318
0 countries
N/A
Brief Summary
The aim of the observational study was to supplement the data on efficacy, safety and tolerability of telmisartan under daily conditions in hospitals
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2000
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2000
CompletedFirst Submitted
Initial submission to the registry
September 11, 2014
CompletedFirst Posted
Study publicly available on registry
September 12, 2014
CompletedSeptember 12, 2014
September 1, 2014
7 months
September 11, 2014
September 11, 2014
Conditions
Outcome Measures
Primary Outcomes (2)
Change in clinic blood pressure
up to 14 days
Number of patients with adverse drug reactions
up to 14 days
Study Arms (1)
essential hypertension patients
Interventions
Eligibility Criteria
Patients with essential hypertension being treated in hospitals
You may qualify if:
- Patients with diagnosis of essential hypertension
- Minimum age of 18 years
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 11, 2014
First Posted
September 12, 2014
Study Start
May 1, 2000
Primary Completion
December 1, 2000
Last Updated
September 12, 2014
Record last verified: 2014-09