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Study to check safety and effectiveness of cilnidipine, metoprolol succinate and chlorthalidone in Indian hypertensive patients.

Not Applicable
Conditions
Health Condition 1: I10- Essential (primary) hypertension
Registration Number
CTRI/2019/01/017089
Lead Sponsor
Aprica Healthcare Pvt Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Patients willing to provide written informed consent form

2.Male or Female patients aged 18 years and above

3.Essential hypertension which is uncontrolled (defined as systolic BP >= 140 mmHg or diastolic BP >= 90 mmHg ) on dual anti-hypertensive agents

4.Patients treated with cilnidipine, metoprolol succinate and chlorthalidone

Exclusion Criteria

1. Patients receiving any other antihypertensive other than cilnidipine, metoprolol succinate and chlorthalidone

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. Reduction in Mean Systolic blood pressure <br/ ><br>2. Reduction in Mean Diastolic blood pressure <br/ ><br>3. Complications <br/ ><br>Timepoint: 1, 3 and 6 months
Secondary Outcome Measures
NameTimeMethod
1.Demographic data of study participants <br/ ><br>2.Socioeconomic status of patient <br/ ><br>3. Comorbid conditions <br/ ><br>4.Preferred Dose of cilnidipine, metoprolol succinate and chlorthalidone <br/ ><br>5. Dosage frequency <br/ ><br>6. Administration time <br/ ><br>7. Concomitant medications <br/ ><br>8. Adverse events <br/ ><br>Timepoint: 1, 3 and 6 months
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