Clinical Trials Directory

Trials / Terminated

TerminatedNCT02498444

Perioperative Treprostinil in Pediatric Patients Undergoing the Fontan Operation

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
34 (actual)
Sponsor
Stanford University · Academic / Other
Sex
All
Age
1 Year – 18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to test the efficacy of treprostinil (TRE) in the perioperative non-fenestrated, extracardiac Fontan patients in order to reduce duration of chest tube drainage (in days). The Fontan operation is performed for patients with single ventricle physiology as the final palliation to create a series circulation, with passive systemic venous return to the pulmonary arteries and the single ventricle solely providing systemic output. Patients undergoing extracardiac Fontan tend to have elevation of Fontan pressures immediately following the operation with inflammation from surgery requiring additional fluid administration to maintain blood pressure. Increased Fontan pressures and fluid overload lead to prolonged chest tube drainage. The hypothesis is that treprostinil, a prostacyclin drug that dilates the pulmonary arteries, will improve immediate postoperative Fontan pressures. Treprostinil is not FDA approved for this use. Anecdotally and in a small case series, prostacyclin therapy has been shown to assist in transitioning patients off nitric oxide. The investigators believe that this improvement in hemodynamics will decrease duration of chest tube drainage resulting in a shorter length of hospital stay.

Detailed description

In order to understand the effect of treprostinil on Fontan patients, this study has two parts: 1. reactivity testing with inhaled treprostinil in the cardiac catheterization lab for pre-Fontan patients undergoing routine catheterization in anticipation of the Fontan operation; 2. perioperative use of subcutaneous treprostinil starting immediately pre-op until postoperative day #7 to improve immediate postoperative hemodynamics and ultimately reduce overall length of hospital stay. The investigators hope to learn how pulmonary vasodilator therapy affects and/or improves post- operative hemodynamics following the Fontan operation. This knowledge would be very important in the care of single ventricle patients following the Fontan operation if there is improvement of immediate outcomes and reduction of hospital length of stay. On a broader scale, if the use of treprostinil in perioperative Fontan patients can achieve the same results other centers achieve with the use of a fenestration this may have wide scale implications in the nationwide treatment of Fontan patients.

Conditions

Interventions

TypeNameDescription
DRUGTreprostinilAdministration of drug (treprostinil) vs placebo (saline) in the post-operative period

Timeline

Start date
2015-09-01
Primary completion
2020-12-01
Completion
2020-12-01
First posted
2015-07-15
Last updated
2022-03-31
Results posted
2022-03-31

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02498444. Inclusion in this directory is not an endorsement.

Perioperative Treprostinil in Pediatric Patients Undergoing the Fontan Operation (NCT02498444) · Clinical Trials Directory