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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02222077
Other study ID # Central BP-TOD
Secondary ID
Status Recruiting
Phase N/A
First received August 15, 2014
Last updated September 13, 2017
Start date July 2014
Est. completion date February 2018

Study information

Verified date September 2017
Source University of Athens
Contact George S Stergiou, Professor of Medicine
Phone +302107763117
Email gstergi@med.uoa.gr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study aims to investigate in adolescents and young adults:

- the 24h diurnal variation of ambulatory central blood pressure

- the association of central compared to peripheral blood pressure with indices of asymptomatic target-organ damage


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date February 2018
Est. primary completion date February 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 12 Years to 25 Years
Eligibility Inclusion Criteria:

- Adolescents and young adults (age range 12-25 years)

Exclusion Criteria:

- Subjects with any acute or significant chronic disease, with evidence of secondary hypertension, or on regular drug treatment will be excluded

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Greece Hypertension Center, 3rd University Department of Medicine, Sotiria Hospital Athens Attica

Sponsors (1)

Lead Sponsor Collaborator
University of Athens

Country where clinical trial is conducted

Greece, 

Outcome

Type Measure Description Time frame Safety issue
Primary Correlation coefficients (r) between 24h ambulatory central blood pressure and indices of target-organ damage Correlation coefficients (r) will be determined for the relationship between central blood pressure and indices of target-organ damage (left ventricular mass index, carotid intima-media thickness, pulse wave velocity). Also, these coefficients will be compared with z-statistic with the respective ones for the peripheral blood pressure. Assessment of each individual will require up to 3 days
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