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Exercise Hemodynamic, Right Ventricular Coupling and Echocardiography in Pulmonary Hypertension (EXERTION)

U

University of Giessen

Status

Completed

Conditions

Hypertension, Pulmonary
Hypertension, Pulmonary Arterial

Treatments

Other: Exercise

Study type

Observational

Funder types

Other

Identifiers

NCT04663217
AZ 11716

Details and patient eligibility

About

This study aims to investigate the exercise profile in pulmonary hypertension patients with either pulmonary arterial hypertension, chronic thromboembolic pulmonary hypertension or pulmonary hypertension due to left heart disease and in disease control.

Full description

This is a dual-center observational prospective study in patients with pulmonary arterial hypertension, chronic thromboembolic pulmonary hypertension, pulmonary hypertension due to left heart disease. Patients undergoing right heart catheterisation due to dyspnoe with invasive exclusion of pulmonary hypertension will be recruited as disease control.

The study comprises a 1-day screening period, followed by a right heart catheterization with exercise challenge.

The study starts with screening, information of the patients and Informed Consent Form signature at day -1. Screening and inclusion of the patient can be performed on the same day. On the day of the planned right heart catheterization based on clinical grounds, exercise right heart catheterisation (RHC) using Swan-Ganz and/or Conductance catheters with simultaneous echocardiography will be performed. End of study is defined as a complete exercise RHC. Adverse events will be assessed until 1 day after the exercise RHC.

After placement of the Swan-ganz or Conductance catheter patients will undergo an exercise challenge using the following protocol in semi-supine position until exhaustion:

  • Incremental workload increase of 20Watt every 2-4 min.
  • For patients not able to start a 20 Watt, initial workload can be adjusted to a minimum of 5 Watt with 5 Watt increase every 2-4 min until exhaustion
  • Maximal exercise duration is 10-12 minutes
  • Symptoms of dyspnoea during exercise will be rated by subjects at baseline, after 6 minutes and at maximum according to the Borg perceived dyspnoea (0-10) scale.

Simultaneously, echocardiography and lung ultrasound will be performed before exercise (baseline), after 6 minutes of exercise and at maximum.

After assessment of right ventriclure pressure-volume loops during maximum exercise, guided by echocardiographic the conductance catheter will be placed in the right atrium to obtain right atrium pressure-volume loops during maximum exercise.

Optional, the exercise RHC will be performed without the Conductance catheter and only with the Swan-Ganz catheter. In this case, pressure values and cardiac output will be measured using the thermodilution method, averaging 3-5 measurements at baseline, 6 minutes and maximum. Detailed assessment of right atrial pressure curves (with a and v wave) will be performed at baseline, 6 minutes and maximum exercise.

Enrollment

120 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Confirmed diagnosis of pulmonary arterial hypertension (World Health Organization group 1)
  • Pulmonary hypertension due to left heart disease (World Health Organization group 2)
  • Chronic thromboembolic pulmonary hypertension (World Health Organization group 4)
  • Invasive exclusion of pulmonary hypertension
  • Age ≥ 18 years
  • Planned right heart catheterization based on clinical grounds
  • Stable specific PAH medications
  • Ability to undergo cycle ergometry
  • Signed informed consent

Exclusion criteria

  • Other etiologic groups of pulmonary hypertension (World Health Organization group 3, 5)
  • Unstable or severe coronary artery disease
  • Uncontrolled arterial hypertension
  • Left ventricular ejection fraction < 30%
  • Severe congenital or acquired valvular or myocardial disease
  • Progressive left heart failure
  • History of severe ventricular arrhythmias
  • Severe, terminal renal impairment
  • Severe obstructive or restrictive lung disease
  • Severe lung emphysema or interstitial lung disease

Trial design

120 participants in 4 patient groups

Pulmonary arterial hypertension
Description:
Patients with mean pulmonary arterial pressure above 25 mmHg, and a pulmonary capillary wedge pressure below 15 mmHg classified into group 1 of the clinical classification of pulmonary hypertension.
Treatment:
Other: Exercise
Pulmonary hypertension due to left heart disease
Description:
Patients with mean pulmonary arterial pressure above 25 mmHg, and a pulmonary capillary wedge pressure above 15 mmHg with left heart disease, classified into group 2 of the clinical classification of pulmonary hypertension.
Treatment:
Other: Exercise
Chronic thromboembolic pulmonary hypertension
Description:
Patients with mean pulmonary arterial pressure above 25 mmHg, and a pulmonary capillary wedge pressure below 15 mmHg with a history of pulmonary embolism, classified into group 4 of the clinical classification of pulmonary hypertension.
Treatment:
Other: Exercise
Control
Description:
Patients with mean pulmonary arterial pressure below 25 mmHg, and a pulmonary capillary wedge pressure below 15 mmHg with exclusion of pulmonary hypertension.
Treatment:
Other: Exercise

Trial contacts and locations

2

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Central trial contact

Richter J Manuel, MD

Data sourced from clinicaltrials.gov

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