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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04663217
Other study ID # AZ 11716
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 1, 2020
Est. completion date November 4, 2023

Study information

Verified date May 2024
Source University of Giessen
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 120
Est. completion date November 4, 2023
Est. primary completion date November 4, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Intervention

Other:
Exercise
After placement of the right heart catheter patients will undergo an exercise challenge in semi-supine position until exhaustion

Locations

Country Name City State
Germany Kerckhoff-Klinik Bad Nauheim Hesse
Germany University of Giessen Gießen Hesse

Sponsors (1)

Lead Sponsor Collaborator
University of Giessen

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary exercise pulmonary arterial pressure mean pulmonary arterial pressure (mmHg) 1 day
Primary exercise cardiac output cardiac output (l/min); 1 day
Primary exercise pulmonary wedge pressure pulmonary arterial wedge pressure (mmHg) 1 day
Primary exercise arterial elastance arterial elastance (mmHg/mL) 1 day
Primary exercise end-systolic elastance end-systolic elastance (mmHg/mL) 1 day
Primary exercise mean right atrial pressure mean right atrial pressure (mmHg) 1 day
Primary exercise right atrial function right atrial strain (%) 1 day
Primary exercise right volume right ventricular volume (ml) 1 day
Primary exercise right ventriculare function right ventricular strain (%) 1 day
Primary exercise right atrial volume-pressure curves atrial volume to pressure ratio (ml/mmHg) 1 day
Secondary exercise lung congestion B-Lines 1 day
Secondary exercise left atrial function left atrial strain (%) 1 day
Secondary exercise left atrial volume left atrial volume (ml) 1 day
Secondary exercise hepatic backflow diameter inferior vena cava (mm) 1 day
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