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A Comparitive Study to Evaluate the Efficacy and Safety of Chlorthalidone with Losartan versus Amlodipine with Losartan in Patients With Primary Hypertension

A Comparative Study to Evaluate the Efficacy and Safety of Chlorthalidone with Losartan versus Amlodipine with Losartan in Patients With Primary Hypertension

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/03/041375
Enrollment
80
Registered
2022-03-24
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Intervention1: Chlorthalidone with Losartan: Patients to receive Chlorthalidone + Losartan 12.5/50 mg/day, can be escalated to 25/100 mg/day once daily at night for 8 weeks Control Intervention1: Amlo

Sponsors

BMCRI
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient willing to give written informed consent 2.Patients who are diagnosed to be having Stage 2 hypertension as per JNC 8 guidelines

Exclusion criteria

Exclusion criteria: 1.Patients having comorbidities like Chronic kidney disease, Stroke , Congestive Heart Failure, Myocardial infarction , Coronary Artery Disease, Psychiatric Disorders, Suspected Secondary Hypertension (Eg. Renal artery stenosis, Cushingââ?¬•s syndrome ) 2.Pregnant and Lactating mothers 3.Patients with hypersensitivity to the study medications

Design outcomes

Primary

MeasureTime frame
Mean reduction in systolic/diastolic blood pressure after 8 weeks of therapyTimepoint: Baseline , 4 weeks and 8 weeks

Secondary

MeasureTime frame
Patients achieving Target Blood pressure of � 140/90 mmHg Timepoint: 8 weeks

Countries

India

Contacts

Public ContactMamatha K

Bangalore Medical College and Research Institute

koteshwarkamath@yahoo.com9241716884

Outcome results

None listed

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