Skip to content

The Prevalence of Sympathetic Overactivity in Primary Hypertensive Patients.

A Non Interventional, Cross Sectional, Study on the Prevalence of Sympathetic Overactivity in Hypertensive Patients.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01295021
Acronym
SORT
Enrollment
1514
Registered
2011-02-14
Start date
2011-02-28
Completion date
2012-02-29
Last updated
2013-06-10

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

Conditions

Essential Hypertension

Keywords

The prevalence of sympathetic overactivity in hypertensive patients.

Brief summary

The purpose of this NIS is to assess the prevalence of sympathetic overactivity in patients with newly diagnosed essential hypertension.

Detailed description

MC MD

Interventions

None listed

Sponsors

AstraZeneca
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Newly diagnosed essential hypertension patients will be eligible for the study. * Average of two or more systolic BP readings ≥ 140mmHg or diastolic BP readings ≥ 90mmHg

Exclusion criteria

* History of coronary artery disease * History of diabetes

Design outcomes

Primary

MeasureTime frame
Prevalence of SO in newly diagnosed hypertensive patientsVisit 1-3: heart rate & Blood pressure, treatment presribed by physician. The interval between visit 1 and visit 2 is upto 4 weeks and interval between visit 2 & visit 3 is upto 4 weeks depending on Investigators discretion.

Secondary

MeasureTime frame
Association of SO and heart rate.Visits 1-3
Subjective symptoms noticed by the doctor.1st visit
To record the drugs used in the treatment of patients diagnosed with hypertension.Visits 1-3

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026