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Evaluation of efficacy (reduction of blood pressure) and safety( adverse events) of Benidipine, Amlodipine and Telmisartan" anti- hypertensive drugs" in Patients of Hypertension - A comparative study.

Evaluation of Efficacy and Safety of Benidipine, Amlodipine and Telmisartan in Patients of Hypertention- A Comparative Study.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2020/03/024384
Enrollment
207
Registered
2020-03-31
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: I10- Essential (primary) hypertension

Interventions

Control Intervention1: anti-hypertensive drug: Telmisartan Control Intervention2: Anti-hypertensive drug: Tab. Benidipine 4mg OD PO 3months Control Intervention3: Anti-hypertensive drug: Tab. Amlodipi

Sponsors

AIIMS Patna
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Newly diagnosed hypertensive patient. 2) Age: >=30 years to 3) BMI: >18.5 to 4) Sex: Both. 5) Systolic Blood Pressure: >=140 to 6) Diastolic Blood Pressure: >=90 to

Exclusion criteria

Exclusion criteria: 1) Age: =60yrs. 2) BMI: 30 kg/m2. 3) Patients diagnosed with secondary hypertension. 4) Patients with renal disease (serum creatinine >1.2). 5) Patients with any history of drug allergies with anti-hypertensive agents. 6) Patients on any other anti-hypertensive drugs (ACEI/DIURETICS/BETA-BLOCKERS). 7) Patients with liver diseases (ALT/AST 8) Patients with pre-existing pedal edema, hypoproteinemia, and Nephrotic syndrome. 9) Patients with any other chronic illness (Diabetes, Rheumatoid arthritis, Tuberculosis). 10) On long term NSAID and steroids. 11) Patients with unsound mind and drug addicts. 12) Pregnant and lactating women. 13) Patient not willing to give consent.

Design outcomes

Primary

MeasureTime frame
Efficacy-B.P(Day 1, day 15, 1 monthand at 3rd month) Safety -Lipid profile,LFT day 1 and after 3month) Safety-ADRTimepoint: one year

Secondary

MeasureTime frame
cost- effectiveness Quality of life at Day 1 and after 3 monthsTimepoint: one year;effect of drugs on lipid profile, liver function test and renal function test at Day 1 and at 3rd month.Timepoint: one year

Countries

India

Contacts

Public ContactDr Aakanksha Priya

MBBS, MD

drprempgupta@gmail.com7763800139

Outcome results

None listed

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