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NCT Number: NCT06770023

Bridge to Lung Transplant With Trans-septal Extra-corporeal Membrane Oxygenation (ECMO) for Right Heart Failure From Pulmonary Hypertension

The purpose of this study is to determine if transseptal extra-corporeal membrane oxygenation (ECMO) can bridge pulmonary hypertension- right heart failure (PH-RVF) patients to lung transplant safely.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Mayo Clinic in Florida

Jacksonville, Florida, 32224, United States

Location status: Recruiting

Location contact

Ian A Makey

PRINCIPAL_INVESTIGATOR

Ian Makey, MD

CONTACT

[email protected]

800-634-1417

About this study

Results will be released as a manuscript once it has gone through the peer review process. Results will be released even in the event of negative outcomes and the release will be hastened if the study is terminated early.

Medicare beneficiaries may be affected by the device under investigation if they are candidates for lung transplant. Since this is such a select group of patients, we do not expect the results of this trial to be generalizable to the general Medicare population.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Patients that are listed for lung transplantation and have:

  • PH defined as:
  • Group 1 Pulmonary arterial hypertension (PAH): Mean pulmonary artery pressure (PAP) ≥ 20 mm Hg, pulmonary capillary wedge pressure (PCWP) < 15 mm Hg, and pulmonary vascular resistance (PVR) ≥ 3 Wood units
  • Group 3 PH is defined as the presence of chronic lung disease (CLD) and/or hypoxia and mean pulmonary artery pressure (PAP) ≥ 20 mm Hg.
  • Secondary PH (WHO Group 3) or diagnosis of primary PH (WHO Group 1) (to include Eisenmenger syndrome).
  • Failing right ventricle function defined as:
  • a cardiac (CI) index < 2.2 L/min/m^2 despite continuous infusion of high dose inotropes defined as:
  • Inhaled nitric oxide > 20 ppm and one of the following:
  • Dobutamine > 10 ug/kg/min x 15 minutes or
  • Milrinone > 0.5 ug/kg/min x 120 minutes or
  • Epinephrine > 0.5 ug/kg/min x 15 minutes or
  • Norepinephrine > 0.5 ug/kg/min x 15 minutes and have one of the following:
  • central venous pressure (CVP) > 15 mm Hg
  • global RV dysfunction on echocardiography defined as one of the following:
  • a tricuspid annular plane systolic excursion score of <14mm
  • an RV diameter at base >42mm
  • RV short-axis or midcavity diameter >35mm
  • Lactate greater than 3 mmol/L
  • Urine output < 0.5 ml/kg/hour
  • Age > 18 years old
  • BMI <35
  • Informed consent signed by self or legally authorized representative.

Exclusion criteria

  • INTERMACS 1 patients (Critical cardiogenic shock patient who is "crashing and burning", has life-threatening hypotension and rapidly escalating inotropic or pressor support, with critical organ hypoperfusion often confirmed by worsening acidosis and lactate levels)
  • End organ failure defined as: hepatic total bilirubin >5 mg/dL based on lab data within 24 hours prior to transseptal ECMO initiation; renal creatinine >4 mg/dLbased on lab data within the 24 hours prior to transseptal ECMO initiation
  • Evidence of acute neurologic injury
  • Active infection defined as two of the following WBC >12,500, positive blood culture, fever
  • RA thrombus
  • Thrombolysis within the previous 30 days or known existing coagulopathy such as thrombocytopenia or hemoglobin diseases such as sickle cell anemia or thalassemia
  • Right heart failure from isolated pulmonary embolism
  • Right heart failure from coronary artery disease or from left heart failure (WHO Type 2)
  • Congenital forms of pulmonary hypertension such as tetralogy of fallot or pulmonary vein stenosis.

Treatment and study plan

Protek Solo Transseptal Cannula

Device

The Protek Solo Transseptal Cannula ECMO cannula will be placed from the right femoral vein and the drainage cannula will be placed from either the left femoral vein or the right internal jugular vein.

Primary outcomes

  1. Survival until transplant

    Time frame: 3 weeks

    Number of subjects to survive between placement of cannula and lung transplant.

Secondary outcomes

  1. Number of subjects to experience adverse events

    Time frame: 2 months

    Adverse events are defined as: death, major bleeding, failure to achieve left atrium access, device migration and stroke.

  2. Extra-corporeal membrane oxygenation (ECMO) support

    Time frame: 2 months

    Number of days after transplant on ECMO support

  3. Dialysis

    Time frame: 2 months

    Number of subjects who need dialysis after transplant

  4. Hospital Discharge

    Time frame: 2 months

    Number of patients that are successfully discharged from the hospital

Study contacts

Contact information is provided by the study sponsor or research team.

Ian A Makey, MD

CONTACT

[email protected]

9049531048

Mohammad E Alomari, MD

CONTACT

[email protected]

9044283665

Sponsors and collaborators

Lead sponsor

Mayo Clinic

Other

Registry information

Official study title

A Pilot Study of Transseptal ECMO With the Protek Solo Cannula in Lung Transplant Candidates With Right Heart Failure From Pulmonary Hypertension

Important dates

Study start
2026
Primary completion
2027
Study completion
2028
First posted
Jan 13, 2025
Registry last updated
Mar 31, 2026

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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