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UnknownNCT04292483

Pulmonary Capillary Recruitment in Fontan Patients

Pulmonary Capillary Recruitment With Pulmonary Vasodilator Therapy in Patients With Univentricular Heart Physiology and Failing Total Cavo-pulmonary Connection.

Status
Unknown
Phase
Study type
Observational
Enrollment
15 (estimated)
Sponsor
Jewish General Hospital · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

This study evaluates the effects of pulmonary vasodilator therapy on pulmonary capillary blood flow by measuring the functional capillary surface area (FCSA) at baseline and post nitric oxide inhalation, through the injection of 3H-benzoyl-Phe-Ala-Pro (BPAP). FCSA will be related to flow and other hemodynamic parameters in order to determine if there is capillary recruitment or distention in Fontan patients. We will also compare baseline FCSA measurements with previously studied normal subjects, to assess the difference in hemodynamic pulmonary functional parameters between these single ventricle physiology patients and normal subjects.

Conditions

Interventions

TypeNameDescription
DRUGNitric OxideInhaled vasodilator to increase pulmonary capillary perfusion

Timeline

Start date
2020-06-11
Primary completion
2023-12-31
Completion
2023-12-31
First posted
2020-03-03
Last updated
2022-04-07

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT04292483. Inclusion in this directory is not an endorsement.

Pulmonary Capillary Recruitment in Fontan Patients (NCT04292483) · Clinical Trials Directory