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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00286884
Other study ID # MED.RES.HOS.2003.01.LBM
Secondary ID
Status Completed
Phase N/A
First received February 3, 2006
Last updated September 8, 2006

Study information

Verified date September 2006
Source Regional Hospital Holstebro
Contact n/a
Is FDA regulated No
Health authority Denmark: Ethics Committee
Study type Observational

Clinical Trial Summary

The aim of the study is to investigate heart rate variability in patients with white coat hypertension and patients with essential hypertension.


Recruitment information / eligibility

Status Completed
Enrollment 65
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 30 Years to 70 Years
Eligibility Inclusion Criteria:

- age 30-70 years

- office BP >150/95 mmHg and 24-h ambulatory BP =/>135/85 mmHg

- office BP >150/95 mmHg and 24-h ambulatory BP <135/85 mmHg

- office BP <150/95 mmHg and 24-h ambulatory BP <135/85 mmHg

Exclusion Criteria:

- Clinical signs of disease of the heart, lungs, liver, kidneys, brain or endocrine organs

- neoplastic disease

- daily use of medicine

- alcohol abuse

- abnormal laboratory screening including blood-hemoglobin, blood-white cell count, plasma-creatinine, plasma-alanine-amino-transaminases, plasma-albumin, plasma-sodium, plasma-potassium, urinary glucose, urinary albumin; electrocardiogram

- pregnancy

- unwillingness to participate

Study Design

Observational Model: Case Control, Time Perspective: Cross-Sectional


Intervention

Procedure:
Monitoring of heart rate variability


Locations

Country Name City State
Denmark Department of Medical Research, Holstebro Hospital Holstebro

Sponsors (1)

Lead Sponsor Collaborator
Regional Hospital Holstebro

Country where clinical trial is conducted

Denmark, 

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