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Completed

NCT Number: NCT04615754

Ketones for Pulmonary Hypertension - Effects on Hemodynamics

In the present study, patients with idiopathic pulmonary hypertension (IPAH) and chronic thromboembolic pulmonary hypertenion will be investigated in a randomized cross-over design with ketone infusions and placebo. Invasive and non-invasive hemodynamics will be evaluated

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Dept. of cardiology, Aarhus University hospital Skejby,

Aarhus, Region Midjylland, 8200, Denmark

About this study

Pulmonary hypertension (PH) is a debilitating disease that affects both the pulmonary vasculature and the heart. It is associated with increased mortality and hospitalization and impairs daily life for the affected patients. Despite substantial advances in treatment within the past decade the prognosis remains poor with an 1-year mortality of more than 10%.1 The pathophysiology of PH is multifactorial and can be caused by left sided cardiac disease, pulmonary pathophysiological changes in the pulmonary vessels, respiratory diseases and pulmonary embolism.The treatment is targeted at the underlying cause. Hence, left sided heart disease is treated with anticongestive medications4 and respiratory disease by pulmonary medications. However, pulmonary vascular diseases such as chronic thromboembolic pulmonary hypertension (CTEPH) and idiopathic pulmonary arterial hypertension (IPAH) are treated with pulmonary endarterectomy and vasodilators targeting the pulmonary vasculature, respectively. However, not all patients have an optimal pulmonary hemodynamic response on treatment. If patients are left with persistent pulmonary hypertension the disease may progress further and cause right heart failure which worsens the prognosis.

Data from a recent study conducted at the investigator's institution demonstrated 40% increase in cardiac output during infusion of the ketone body 3-hydroxybutyrate (3-OHB). Intriguingly, this was associated with an increase in RV function and a decrease in the pulmonary vascular resistance of approximately 20%.

In the present study, 10 patients with IPAH and 10 patients with CETPH will be subjected to placebo and 3-OHB infusion in a randomized cross-over design. Each of the infusions will be given for 2.5 hours and cross-over will be carried out on the same day. Echocardiography and right sided heart catheterization will be applied and blood will be sampled.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Persistent pulmonary hypertension (defined as PVR > 3 WU, pulmonary capillary wedge pressure (PCWP) < 15 mmHG, mean pulmonary arterial pressure (mPAP) ≥25 mmHg) on the most resent right heart catheterization.
  • Preserved left ventricular ejection fraction (<50%) on most recent echocardiography
  • Able to give informed consent

Exclusion criteria

  • Other Significant pulmonary, mitral or aortic valve disease
  • Other disease or treatment making subject unsuitable for study participation

Treatment and study plan

Hyperketonemia - use of ketone (3-OHB) infusion

Dietary Supplement

The effect of intravenous ketone supplement

Placebo - use of saline infusion

Dietary Supplement

Saline is infused as an comparator

Primary outcomes

  1. Cardiac output (L/min

    Time frame: changes during the infusion for 2.5 hours compared to 2.5 hours of Saline infusion

    Measured by Swan-Ganz monitoring

Secondary outcomes

  1. mixed venous saturation (%)

    Time frame: changes during the infusion for 2.5 hours compared to 2.5 hours of Saline infusion

    Hemodynamics - Swan Ganz monitoring

  2. systemic blood pressure (mmHg)

    Time frame: changes during the infusion for 2.5 hours compared to 2.5 hours of Saline infusion

    Hemodynamics - non-invasive blood pressure measurement

  3. pulmonary capillary pressure (mmHg)

    Time frame: changes during the infusion for 2.5 hours compared to 2.5 hours of Saline infusion

    Hemodynamics - Swan Ganz monitoring

  4. Pulmonary pressure (mmHg)

    Time frame: changes during the infusion for 2.5 hours compared to 2.5 hours of Saline infusion

    Hemodynamics - Swan Ganz monitoring

  5. TAPSE (mm)

    Time frame: changes during the infusion for 2.5 hours compared to 2.5 hours of Saline infusion

    Echocardiography

  6. RV strain (%)

    Time frame: changes during the infusion for 2.5 hours compared to 2.5 hours of Saline infusion

    Echocardiography

  7. LV strain (%)

    Time frame: changes during the infusion for 2.5 hours compared to 2.5 hours of Saline infusion

    Echocardiography

  8. systolic tricuspid plane velocity (cm/sec)

    Time frame: changes during the infusion for 2.5 hours compared to 2.5 hours of Saline infusion

    Echocardiography

  9. Left ventricular ejection fraction (%)

    Time frame: changes during the infusion for 2.5 hours compared to 2.5 hours of Saline infusion

    Echocardiography

  10. Changes in Prostaglandines (pmol/L)

    Time frame: changes during the infusion for 2.5 hours compared to 2.5 hours of Saline infusion

    Blood samples

  11. pH

    Time frame: changes during the infusion for 2.5 hours compared to 2.5 hours of Saline infusion

    Blood samples

  12. sodium (mM)

    Time frame: changes during the infusion for 2.5 hours compared to 2.5 hours of Saline infusion

    Blood samples

  13. potassium (mM)

    Time frame: changes during the infusion for 2.5 hours compared to 2.5 hours of Saline infusion

    Blood samples

  14. lactate (mM)

    Time frame: changes during the infusion for 2.5 hours compared to 2.5 hours of Saline infusion

    Blood samples

Sponsors and collaborators

Lead sponsor

University of Aarhus

Other

Collaborators

  • Danish Heart Foundation

Registry information

Official study title

Ketone Administration in Patients With Pulmonary Hypertension - Effects on Hemodynamics

Acronym: KEPAH

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Nov 4, 2020
Registry last updated
Dec 2, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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