Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT04849806

Sympathetic Nerve Activity Predictors in Patients With Chronic Obstructive Pulmonary Disease

Led by RWTH Aachen University · Updated on 2026-01-28

135

Participants Needed

1

Research Sites

342 weeks

Total Duration

On this page

Sponsors

R

RWTH Aachen University

Lead Sponsor

D

DFG - Deutsche Forschungs Gemeinschaft (German Research Foundation)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The project will be pursued in our respiratory, autonomic nervous system physiology laboratory (Respiratory, autonomic nervous system physiology laboratory, Department of Pneumology and Intensive Care Medicine, RWTH Aachen University Hospital; Head of Department: Professor Michael Dreher). Overactivity of the sympathetic nerve activity (SNA) axis with "centrally" increased heart rate and peripheral vasoconstriction is a known phenomenon in patients with systolic heart failure (HF) and has recently been described in patients with primary lung disease as seen in chronic obstructive pulmonary disease (COPD). However, systematic analyses on this clinically relevant topic are currently lacking. Thus, using a comprehensive, multimodal approach and state-of-the-art technology, this research project is designed to determine the extent and nature of increased SNA in COPD (AIM 1) and evaluate the underlying mechanisms (AIM 2). The project will address the following hypotheses: 1. In COPD, concomitant obstructive sleep apnea is independently associated with increased SNA. 2. Precapillary pulmonary hypertension (PH), inspiratory muscle dysfunction and systemic inflammation describe a COPD phenotype characterised by increased SNA with a different subtype.

CONDITIONS

Official Title

Sympathetic Nerve Activity Predictors in Patients With Chronic Obstructive Pulmonary Disease

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 218 years or older
  • Ability and willingness to give informed consent to participate in the study
Not Eligible

You will not qualify if you...

  • Atrial fibrillation
  • Active pacing of the heart by a cardiac pacemaker (no intrinsic heart rate)
  • Clinically pre-established cardiovascular disease such as arterial hypertension or systolic heart failure
  • In-patient hospital stay within the last 4 weeks prior to the study examination date

AI-Screening

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Trial Site Locations

Total: 1 location

1

RWTH Aachen University

Aachen, Germany

Actively Recruiting

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Research Team

M

Michael Dreher, Professor

CONTACT

J

Jens Dr. Spiesshoefer, 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

2

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