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UnknownNCT03014791

Influence of Age, Weight and Ethnic Background on Blood Pressure

Influence of Age, Weight and Ethnic Background on Blood Pressure: AWE Study

Status
Unknown
Phase
Study type
Observational
Enrollment
500 (estimated)
Sponsor
Cambridge University Hospitals NHS Foundation Trust · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

Hypertension, also known as high blood pressure, is a chronic medical condition, in which the blood pressure is elevated. This is a common condition, which can lead to severe complications such as cardiovascular disease, heart attack, stroke and kidney disease, if not detected and treated early. Accumulating evidence suggests that the incidence of hypertension varies according to age, ethnicity and obesity. In order to obtain an in-depth knowledge of the pathophysiological mechanisms of hypertension, we aim to investigate the haemodynamic and biochemical correlates of elevated blood pressure across the adult age-span, and determine the extent to which body size and ethnicity impact on these associations. We also wish to investigate the impact of hypertension on key target organs (end-organ damage). The primary objective of this study is to compare the mechanisms regulating blood pressure in hypertensive and non-hypertensive participants across the adult age span, and to assess the influence of body mass index and ethnic background on these mechanisms. Secondary objectives are to investigate the association between blood pressure and cardiovascular physiology across the adult age span at rest and during sub-maximal exercise and to investigate the impact of blood pressure haemodynamics on key organs including the arteries and heart by assessing end-organ damage such as endothelial function, arterial structure and left ventricular mass/function. This study will be a combined case-control and cross-sectional study describing the procedures and time commitment required to investigate our scientific aims. This is a single centre study that will be conducted in a secondary care environment. Both male and females aged 18 and over and that are able provide informed consent will be considered for this study. People who are pregnant, currently receiving dialysis, illness with a life expectancy \<1 year, current active malignancy and cannot provide informed consent are ineligible for this study. The study will be open for five years and each patient will complete a maximum of four visits in a 12 month period. Participants will complete a variety of non-invasive physiological assessments of their cardiovascular system and lung function. There will be some minimally invasive procedures completed, including a blood test and assessment of small artery endothelial function which involves insertion of a small needle under local anesthetic.

Conditions

Interventions

TypeNameDescription
OTHERBrief lifestyle/medical history questionnaireCore Measurement
OTHERAnthropometric measuresCore Measurement
OTHERBlood pressure and arterial stiffnessCore Measurement
OTHERCardiac output and lung functionCore Measurement
OTHERHeart rate variabilityCore Measurement
OTHERBlood sample & spot urine sampleCore Measurement
OTHER24 hour ambulatory blood pressure monitorDetailed Measurement (Optional for participants).
OTHER24 hour urine collectionDetailed Measurement (Optional for participants).
OTHEREchocardiograph: Left ventricular massDetailed Measurement (Optional for participants).
OTHERLarge artery structure: Carotid intima-media thicknessDetailed Measurement (Optional for participants).
OTHERSmall artery structure: Minimum forearm vascular resistanceDetailed Measurement (Optional for participants).
OTHERLarge artery endothelial functionFlow- and salbutamol-mediated vasodilatation Detailed Measurement (Optional for participants).
OTHERSmall artery endothelial function: Forearm blood flowDetailed Measurement (Optional for participants).
OTHERDundee step testSystolic blood pressure response to submaximal exercise Detailed Measurement (Optional for participants).
OTHERDetailed haemodynamic response to submaximal exerciseDetailed Measurement (Optional for participants).
OTHERCardiopulmonary fitness: Maximum oxygen consumptionDetailed Measurement (Optional for participants).
OTHERHaemodynamic response to mental stressDetailed Measurement (Optional for participants).
OTHERSmall artery dilatory function: Forearm blood flowDetailed Measurement (Optional for participants).

Timeline

Start date
2017-02-21
Primary completion
2024-02-01
Completion
2024-02-01
First posted
2017-01-09
Last updated
2022-08-23

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT03014791. Inclusion in this directory is not an endorsement.