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An observational study to assess the central aortic blood pressure readings in adult patients of essential hypertension uncontrolled on single antihypertensive agents in the real world clinical setting.

An observational study to assess the central aortic blood pressure readings in adult patients of essential hypertension uncontrolled on single antihypertensive agents in the real world clinical setting - CAP

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2015/10/006302
Enrollment
2000
Registered
2015-10-23
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- Hypertension Health Condition 2: I119- Hypertensive heart disease withoutheart failure

Interventions

Intervention1: NIL: NIL

Sponsors

Sanofi Synthelabo India Private Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Male or Female patients 30-70 years of age 2. Essential hypertension which is uncontrolled (defined as systolic BP >= 140 mmHg or diastolic BP >= 90 mmHg (7)) on single anti-hypertensive agent 3. Investigators decides to add a second new anti-hypertensive agent 4. Signed Informed consent form obtained prior to initiation of the study

Exclusion criteria

Exclusion criteria: 1. Patient currently participating in a clinical trial 2. Patients unable to comply with the protocol requirements 3. Pregnancy 4. Patients with hypertensive urgencies and emergencies 5. Patients with known case of secondary hypertension 6. Patients with known case of complications due to hypertension

Design outcomes

Primary

MeasureTime frame
Proportion of patients with central systolic pressure 125 mmHg (8) at visit 1Timepoint: 01 Days

Secondary

MeasureTime frame
1) To compare brachial and central aortic blood pressure across various drugs classes at visit 1 and at 8th week ± 7days (visit 2), For details please see the protocol.Timepoint: 8th week ± 7days (visit 2)

Countries

India

Contacts

Public ContactMs Vaishali Kanade

SANOFI -SYNTHELABO (I) PVT LIMITED

Vaishali.Kanade@sanofi.com022-28032823

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 23, 2026