Skip to content

A Comparative Randomized Control Study between Amlodipine and Cilnidipine in mild Hypertensive patients to evaluate the efficacy and safety of the two drugs in cardiology outpatient department of tertiary care hospital

A Comparative Randomized Control Study between Amlodipine and Cilnidipine in Grade-I Hypertensive patients to evaluate the efficacy and safety of the two drugs in cardiology outpatient department of tertiary care hospital

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/08/015150
Enrollment
200
Registered
2018-08-01
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Grade-I Hypertensive patients

Interventions

Intervention1: Cilnidipine: 10mg oral tablet once daily in morning for 52 weeks Control Intervention1: Amlodipine: 5mg oral tablet once daily in morning for 52 weeks

Sponsors

NRS Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Newly diagnosed case of gradeI hypertension 2 Adult age group from 18 yrs to 80 yrs 3 Patients willing to give written consent 4 Hypertensive patients without other co morbid factors like angina cardiac ischemia cerebrovascular disease peripheral vascular disease cardiac infarction renal disease preexisting edema corpulmonale anaemia hypoproteinemia nephrotic syndrome hepatic cirrhosis

Exclusion criteria

Exclusion criteria: 1 Patients taking NSAIDS and Amantadine 2 Patients taking other anti hypertensive drugs 3 Pregnancy 4 Patients taking antipsychotic drugs 5 Patients taking drugs that cause Pedal Edema 6 Patients not responding in treatment during 2 weeks 7 Patients taking less than 30 percent of the tablets dispensed as study medication

Design outcomes

Primary

MeasureTime frame
1 Changes Of systolic Blood Pressure From baseline to normal 2 Changes Of Diastolic Blood Pressure From Baseline to normalTimepoint: 52 weeks after starting of treatment

Secondary

MeasureTime frame
1 Heart rate changes 2 Changes in ecg 3 Changes in estimated glomerular filtration rate 4 Changes in albumin creatinine ratio 5 Changes in echocardiography Timepoint: 52 weeks after starting of treatment

Countries

India

Contacts

Public ContactDr Priyatosh Saha

NRS MEDICAL COLLEGE

drninadas@yahoo.com09433165691

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026