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The Role of the Pulmonary Vasculature in the Fontan Circulation

U

University Medical Center Groningen (UMCG)

Status

Enrolling

Conditions

Pulmonary Vascular Remodeling
Pulmonary Vascular Resistance
Fontan Operation
Congenital Heart Disease

Study type

Observational

Funder types

Other

Identifiers

NCT02414321
NL51128.042.15

Details and patient eligibility

About

This study aims to explore the structural and functional characteristics of the pulmonary vasculature in adult Fontan patients.

Objectives:

  • Determine the effect of pulmonary vasodilatation on indexed cardiac output during simulated exercise.
  • Characterization of structural properties of small pulmonary arteries.

Full description

Rationale:

The Fontan circulation is a palliation for patients with a functionally univentricular heart. The Fontan circulation is characterized by impaired exercise capacity and gradual attrition over time. To date treatment options are extremely limited. It has been proposed that pulmonary vascular resistance (PVR) is the controlling and limiting factor of cardiac output in the Fontan circulation. Remodeling of the pulmonary vasculature and increasing PVR are possible key factors in the long term failure of the Fontan circulation. Optical Coherence Tomography (OCT) is an intravascular imaging modality used for structural characterization of blood vessels. Nitric oxide is a pulmonary vasodilator used in pulmonary vascular response tests, aimed at lowering PVR which may improve cardiac output in the Fontan circulation. These two diagnostic procedures are tools to study the structural and functional characteristics of the pulmonary vasculature in the Fontan circulation. The results of this study could identify the pulmonary circulation as a future treatment target in Fontan patients and may provide clues for new therapeutic treatment strategies to improve the long term outcome of these patients.

Study procedure:

The study protocol will be performed during a clinically indicated cardiac catheterization. In the context of this study additional measurements will be performed which will include a pulmonary vascular response test, trans-thoracic echocardiography and pulmonary artery OCT measurements.

Enrollment

20 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Fontan group

  • written informed consent
  • Clinical indication for cardiac catheterization

Control group

  • written informed consent
  • Clinical indication for right heart catheterization
  • Absence of pulmonary vascular disease
  • Normal pulmonary vascular hemodynamic profile

Exclusion criteria

Fontan group

  • Standard exclusion criteria for cardiac catheterization
  • Obstruction in Fontan conduit
  • Inability to measure a reliable cardiac index and PVR (rhythm instability, hemodynamic or anatomic reasons)

Control Group

  • No specific exclusion criteria apart from the standard exclusion criteria for right heart catheterization.

Trial design

20 participants in 3 patient groups

Fontan group
Description:
Right heart catheterization: * pulmonary artery OCT analysis * dobutamine stress test * pulmonary vascular response test (nitric oxide) * trans-thoracic echocardiography
Control group
Description:
Right heart catheterization: - pulmonary artery OCT analysis
PAH group
Description:
Right heart catheterization: - pulmonary artery OCT analysis

Trial contacts and locations

1

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Central trial contact

Floris-Jan S Ridderbos, MD; Elke S Hoendermis, MD PhD

Data sourced from clinicaltrials.gov

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