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Arterial Stiffness, Blood Pressure and Cardiac Output Study (ABC)

Primary Purpose

Infrarenal Abdominal Aortic Aneurysm

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Pulse wave analyses; central blood presaure parameters
Sponsored by
Rijnstate Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Infrarenal Abdominal Aortic Aneurysm focused on measuring EVAR, central pressure, arterial stiffness, AAA, elective surgery

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Male or female at least 18 years old;
  2. Informed consent form understood and signed and patient agrees to follow-up visits;
  3. Have a infrarenal abdominal aortic aneurysm (AAA) with maximum sac diameter ≥ 5.5cm, or an AAA ≥ 4.5 cm which has increased by > 1.0 cm in the past year with a scheduled endovascular intervention

Exclusion Criteria:

  1. Life expectancy < 2 years;
  2. Psychiatric or other condition that may interfere with the study;
  3. Participating in another clinical study, interfering on outcomes;
  4. Irregular pulse;
  5. Presence of extensive peripheral arterial disease (ABI < 0.9 or obstruction validated on imaging); dated less than 3 months prior to treatment
  6. Ruptured, leaking or mycotic aneurysm;

Sites / Locations

  • Rijnstate Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

elective EVAR patients

Arm Description

Elective EVAR patients will be included in one arm only

Outcomes

Primary Outcome Measures

central blood pressure
comparison of invasively recorded and non-invsively estimated central blood pressure

Secondary Outcome Measures

changes in arterial stiffness pre- and post EVAR
changes in arterial stiffness pre- and post EVAR
influence of thrombus on arterial stiffness
influence of thrombus on arterial stiffness
changes in arterial stiffness over time
changes in arterial stiffness over time

Full Information

First Posted
March 5, 2018
Last Updated
March 10, 2020
Sponsor
Rijnstate Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03469388
Brief Title
Arterial Stiffness, Blood Pressure and Cardiac Output Study
Acronym
ABC
Official Title
Arterial Stiffness, Blood Pressure and Cardiac Output Study; ABC-study A Prospective, Multidisciplinary Study of Arterial Stiffness Measures in Patients Treated for Aortic Aneurysms in Relation to Blood Pressure and Cardiac Output
Study Type
Interventional

2. Study Status

Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
April 24, 2017 (Actual)
Primary Completion Date
August 5, 2019 (Actual)
Study Completion Date
December 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rijnstate Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Comparison of non-invasively obtained central blood pressure using SphygmoCor and invasively recorded central blood pressure in patients with an AAA that will be treated with EVAR.
Detailed Description
Primary objective of the first study: validation of non-invasive central pressure parameters in patients treated with EVAR against invasive measurements. Objectives of subsequent studies: Do non-invasive central parameters change over time after EVAR? What is the influence of intraluminal thrombus (presence, amount, configuration) on non-invasive central pressure parameters (and other obtained parameters of arterial stiffness)? Prospective study with consecutive, eligible subject enrollment. All subjects will undergo the Endovascular Aneurysm repair procedure with an endovascular device. Subjects will be followed procedurally, at 6-8 weeks and 1 year post implantation. This study is a collaboration of the following departments of the Vascular Center in the Rijnstate Hospital Arnhem: Vascular Surgery, Interventional radiology, Internal Vascular Medicine, Cardiology. Patients diagnosed with an abdominal aortic or aortoiliac aneurysm who are considered candidates for endovascular repair and who meet the study eligibility criteria may be screened for enrollment in the study. Up to 20 subjects will be enrolled . Pre-procedural high resolution, contrast-enhanced CT scan evaluation to determine anatomical eligibility for enrollment will be performed within three months of the study procedure, according to standard care. Following EC/IRB approval of the study and the written informed consent form, patients will be screened for eligibility. Following informed consent, clinical characteristics will be reported (from hospital records). Per-procedural PWA measurements will be performed simultaneously with intravascular pressure measurements pre-implantation and after completion of the endocasular implantation. Subjects will be followed at 30 days and 1 year post-implantation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infrarenal Abdominal Aortic Aneurysm
Keywords
EVAR, central pressure, arterial stiffness, AAA, elective surgery

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
prospective,multidisciplinary single center study
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
elective EVAR patients
Arm Type
Experimental
Arm Description
Elective EVAR patients will be included in one arm only
Intervention Type
Diagnostic Test
Intervention Name(s)
Pulse wave analyses; central blood presaure parameters
Other Intervention Name(s)
Pulse wave velocity
Intervention Description
Pulse wave analyses; central blood presaure parameters
Primary Outcome Measure Information:
Title
central blood pressure
Description
comparison of invasively recorded and non-invsively estimated central blood pressure
Time Frame
one week
Secondary Outcome Measure Information:
Title
changes in arterial stiffness pre- and post EVAR
Description
changes in arterial stiffness pre- and post EVAR
Time Frame
1 year
Title
influence of thrombus on arterial stiffness
Description
influence of thrombus on arterial stiffness
Time Frame
1 year
Title
changes in arterial stiffness over time
Description
changes in arterial stiffness over time
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female at least 18 years old; Informed consent form understood and signed and patient agrees to follow-up visits; Have a infrarenal abdominal aortic aneurysm (AAA) with maximum sac diameter ≥ 5.5cm, or an AAA ≥ 4.5 cm which has increased by > 1.0 cm in the past year with a scheduled endovascular intervention Exclusion Criteria: Life expectancy < 2 years; Psychiatric or other condition that may interfere with the study; Participating in another clinical study, interfering on outcomes; Irregular pulse; Presence of extensive peripheral arterial disease (ABI < 0.9 or obstruction validated on imaging); dated less than 3 months prior to treatment Ruptured, leaking or mycotic aneurysm;
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michel Reijnen, MD, PhD
Organizational Affiliation
Rijnstate
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rijnstate Hospital
City
Arnhem
State/Province
Gelderland
ZIP/Postal Code
6800 TA
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
34585343
Citation
Holewijn S, Vermeulen JJM, van Helvert M, van de Velde L, Reijnen MMPJ. Validation of Central Pressure Estimation in Patients with an Aortic Aneurysm Before and After Endovascular Repair. Cardiovasc Eng Technol. 2022 Apr;13(2):265-278. doi: 10.1007/s13239-021-00574-3. Epub 2021 Sep 28.
Results Reference
derived

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Arterial Stiffness, Blood Pressure and Cardiac Output Study

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