Patients who have been randomized in a prevous clinical trial of telmisartan can participate. Safety will be assessed by physical examinations, vital signs, 12-ECG, laboratory evaluation as well as adverse events. Efficacy will be assessed by supine blood pressure results. The primary objective of this trial is to assess the safety of Telmisartan during open-label, long term treatement. The study will last 2-3 years with 15-20 patients participating.

Project Start
1997-12-01
Project End
1998-11-30
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
38
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Washington University
Department
Type
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
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