The objective is to investigate the safety of ramipril 10 mg/day used in prevention of cardiovascular events in high-risk patients, including the criteria of the HOPE study.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
1,012
tablet of Ramipril once daily
Sanofi-Aventis Administrative Office
Dhaka, Bangladesh
Number of patient reaching the 10mg/day dose level
Time frame: 30 days after the treatment start
Overall number of adverse events
Time frame: at day 7 (visit 2), day 15 (visit 3), day 30 (visit 4), day 45 (visit 5) and day 60 (final visit)
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.