None listed
Conditions
Interventions
None listed
Sponsors
Eris Lifescience Ltd
Heart care Foundation of India National NGO
Eligibility
Inclusion criteria
Inclusion criteria: 1. Male or female subjects aged 18 years and older without a history of hypertension 2. Office systolic blood pressure between 100 and 180 mmHg and diastolic blood pressure between 60 and 110 mmHg
Exclusion criteria
Exclusion criteria: 1. Subjects who are unable or unwilling to take self-measurements of blood pressure at home 2. Subjects who do not sign informed consent 3. Office Blood pressure higher than 180 and 110 mmHg for systolic and diastolic blood pressure, respectively 4. Patients with secondary Hypertension 5. Patients already on Anti-hypertensive medication
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary objective of the study is long term follow up of the natural history of the subjects enrolled for a period of 5 years.Timepoint: 5 years | — |
Secondary
| Measure | Time frame |
|---|---|
| To have better insights on how many normotensive or white coat hypertensive patients turned hypertensive over a course of time and document their natural history. Record any hospitalizations during follow up for HT-related problems – Time period of Diagnosis (Stroke, ACS, Renal failure etc.)Timepoint: 5 years | — |
Countries
India
Contacts
Public ContactDr Viraj Suvarna
Batra hospital & Medical Research Centre
Outcome results
None listed