Actively Recruiting

Age: 18Years +
All Genders
NCT06887101

Impact of Stress on Cardiovascular Events in Patients with Peripheral Arterial Disease

Led by University Hospital, Essen · Updated on 2025-03-20

300

Participants Needed

1

Research Sites

192 weeks

Total Duration

On this page

Sponsors

U

University Hospital, Essen

Lead Sponsor

U

Universität Duisburg-Essen

Collaborating Sponsor

AI-Summary

What this Trial Is About

Atherosclerotic cardiovascular disease is the leading cause of morbidity and mortality worldwide. Patients with peripheral arterial disease are at increased risk suffering from major adverse cardiac and limb events. Acute and chronic stress affect the cardiovascular system. Long-term negative stressors lead to cardiovascular diseases and can aggravate already existing cardiovascular diseases. However, current guidelines on cardiovascular disease prevention highlight stress as a cardiovascular risk factor there is a lack of consensus about the definition and measurement of stress. The aim of the proposed trial is to evaluate different stress measuring methods in patients with PAD depending on the occurrence of cardiovascular events.

CONDITIONS

Official Title

Impact of Stress on Cardiovascular Events in Patients with Peripheral Arterial Disease

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of lower extremity peripheral arterial disease (PAD) based on one or more of the following:
  • Limb bypass surgery
  • Aorta-femoral bypass surgery
  • Percutaneous transluminal angioplasty revascularization of the iliac or infrainguinal arteries
  • Limb or foot amputation for arterial vascular disease
  • Intermittent claudication plus either ankle brachial index (ABI) less than 0.90 or peripheral artery stenosis (≥50%) documented by angiography or duplex ultrasound
  • Carotid revascularization or asymptomatic carotid artery stenosis of at least 50% diagnosed by duplex ultrasound or angiography
Not Eligible

You will not qualify if you...

  • Atrial fibrillation
  • High premature ventricular contractions burden
  • Pacemaker with constant ventricular pacing
  • Use of antiarrhythmic drugs class I or III

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Department of Cardiology and Vascular Medicine, West German Heart and Vascular Center, University Hospital Essen

Essen, Germany, 45147

Actively Recruiting

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Research Team

J

Julia Lortz, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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