A Clinical Study to evaluate the effect of two different combinations of BP medication in patients with uncontrolled BP
- Conditions
- Health Condition 1: I10- Essential (primary) hypertension
- Registration Number
- CTRI/2018/08/015555
- Lead Sponsor
- Current Medical Concepts Pvt Ltd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 93
a) Adults greater than or equal to 18 years and
less than or equal to 70 years old both male
and female.
b) Subjects with uncontrolled BP who are on
monotherapy.
c) Systolic Blood Pressure (SBP) >130 mmHg and
Diastolic Blood Pressure (DBP) > 80
mmHg based on three consecutive blood
pressure readings
d) Any stage of Hypertension.
e) Willing to give written informed consent
a) Women of child bearing potential
b) History of Myocardial infarction, Acute
stroke, Acute kidney injury in the last 3
months
c) Subjects with history of congestive heart
failure.
d) Subjects with advanced CKD with Serum
Creatinine value > 2.5 mg/dL.
e) History of allergy to calcium channel
blockers and angiotensin receptor blockers
f) Inability to give informed consent
g) Subject with hypertensive crisis (Seated BP
greater than or equal to 180/120 mmHg) on
the day of screening.
h) Subjects unwilling/unable to adhere to the
study protocol.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method