Relation betwEen Abdominal Aorta and Carotid Artery Responses to SymPathetic stimulatiON uSing duplEx Ultrasound
RESPONSE
1 other identifier
observational
60
1 country
2
Brief Summary
Abdominal aortic aneurysm (AAA) is a common vascular disease and associated with risk of rupture, but also with a high cardiovascular (CV) event rate. A key difficulty in AAA is predicting these life-threatening complications. Recent studies suggest that the endothelial function of the abdominal aorta might have a correlation with the disease development. A novel, easy to perform, non-invasive test can assess central artery endothelial function (i.e. the carotid artery reactivity (CAR)). The CAR test is based on the cold pressure test (CPT), which induces sympathetic stimulation by placing one hand in cold water. Using duplex ultrasound, central artery blood flow and diameter responses can be examined. Previous work has demonstrated that the CPT is associated with an increase in abdominal aortic diameter, whilst others found that the carotid and coronary artery diameter also shows dilation. Interestingly, a previous study found a strong correlation between carotid and coronary artery diameter responses to the CPT, whilst these artery responses show independent prognostic value for future cardiovascular events in patients with peripheral arterial disease. Possibly, similarity may be present in central artery reactivity to the CPT. To date, no study examined whether carotid and aorta responses are in agreement during the CPT. Given the potential importance of central artery vasoreactivity for AAA, the CAR-test may have potential in this group, especially given the relative simplicity of measuring the carotid artery. The aim of this explorative study is to investigate the correlation between the magnitude of the abdominal aorta and the carotid artery diameter and blood flow responses during the sympathetic stimulation (using the cold pressor test) between healthy young, healthy older and individuals with AAA.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Oct 2019
Shorter than P25 for all trials
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 25, 2019
CompletedFirst Posted
Study publicly available on registry
July 29, 2019
CompletedStudy Start
First participant enrolled
October 1, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
October 5, 2020
CompletedOctober 12, 2020
October 1, 2020
10 months
July 25, 2019
October 9, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
CAR-test
Percentage of vasodilation/vasoconstriction to the CAR test at the common carotid artery
Baseline
CAR-test
Percentage of vasodilation/vasoconstriction to the CAR test at the abdominal aorta
Baseline
Secondary Outcomes (7)
CAR-test
Baseline
CAR-test
Baseline
CAR-test
Baseline
CAR-test
Baseline
CAR-test
Baseline
- +2 more secondary outcomes
Other Outcomes (13)
Demographic characteristics
Baseline
Demographic characteristics
Baseline
Demographic characteristics
Baseline
- +10 more other outcomes
Study Arms (3)
1. Young healthy group
Male or female between the age of 18 and 40 years old. No presence of systolic blood pressure \>140 and/or diastolic blood pressure \>90, cardiovascular history or antihypertensive medication
2. Patients with an AAA
Individuals (\>60 years) with a small, stable, abdominal aortic aneurysm (i.e. AAA diameter of 30-50 mm)
3. Healthy older group
Healthy age- and sex- matched with group 2 with no presence of systolic blood pressure \>140 and/or diastolic blood pressure \>90, cardiovascular history or antihypertensive medication
Interventions
The CAR test will be applied to stimulate the sympathetic nervous system. This thermal stimulus is known to elevate blood pressure via sympathetic pathways, so it can be used to study the vascular response to sympathetic activation. The participant will submerge their left hand in a bucket of ice water (approximately 4 degrees celcius) for 3 minutes, which is reported to be sufficient to induce a maximal dilation in the common carotid artery. At baseline and every minute after the hand is submerged in ice water, the blood pressure will be measured to check whether a sympathetic stimulation is achieved. During this test as well the carotid artery as the abdominal aorta will be visualized using ultrasound.
Eligibility Criteria
1. twenty healthy, young (18-40 years) subjects, 2. twenty older subjects (\>60 years) with a small, stable abdominal aortic aneurysm (i.e. AAA diameter of 30-50 mm), and 3. twenty healthy, age-/sex matched with group 2. We aim to include an equal number of male and females in both groups.
You may qualify if:
- Young healthy group: Male or female between the age of 18 and 40 years old;
- Older healthy group: Male or female, which are age-/sex-matched with the AAA patients group;
- AAA patients group: Male or female with an abdominal aortic aneurysm who is still under surveillance, with a diameter between 3.0 and 5.0 cm and at least 18 years old. These patients may participate in the 1-2-3 Trial, which is a similar approved investigation by CMO region Arnhem-Nijmegen with registration number 2019-5216.
- Informed consent form understood and signed;
You may not qualify if:
- Psychiatric or other conditions that may interfere with the study;
- Participating in another clinical study, interfering on outcomes;
- With regard to the necessary quality of the ultrasound images, BMI ≥ 30 kg/m2;
- Increased risk for coronary spasms (score Rose-questionnaire ≥2; this questionnaire can be found in the Appendix);
- Known carotid artery disease
- Presence of Raynaud's phenomenon, Marfan syndrome, chronic pain syndrome at upper extremity(s), presence of an AV fistula or shunt, open wounds to the upper extremity(s), and/or scleroderma associated with placing the hand in ice water;
- Recent (\<3 months) presence of angina pectoris, myocardial infarction, cerebral infarction, and/or heart failure, or PAD treatment.
- Healthy groups:
- Systolic blood pressure \>140 and/or diastolic blood pressure \>90
- Cardiovascular history
- Antihypertensive medication
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Rijnstate Hospitallead
- Radboud University Medical Centercollaborator
Study Sites (2)
Rijnstate Hospital
Arnhem, Gelderland, Netherlands
Radboudumc
Nijmegen, Gelderland, 6525GA, Netherlands
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Michel Reijnen, MD, Prof
Rijnstate Hospital
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 25, 2019
First Posted
July 29, 2019
Study Start
October 1, 2019
Primary Completion
August 1, 2020
Study Completion
October 5, 2020
Last Updated
October 12, 2020
Record last verified: 2020-10