MedTrace Logo

Ocular and Vision Problems in Patients After Fontan Operation

NCT03170778 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 65

Last updated 2022-05-04

No results posted yet for this study

Summary

The purposes of this study are to identify indicators of vision problems and ocular abnormalities in patients with a Fontan circulation through a standardized questionnaire and to correlate the intraocular pressure measured with the Icare tonometer with central venous pressure measured with the VENUS 2000 CVP non-invasive system to determine whether intraocular pressure can be used as a surrogate measure of increased central venous pressure in patients with a Fontan circulation.

Conditions

  • Congenital Heart Disease

Sponsors & Collaborators

Principal Investigators

  • Susan Fernandes, LPD, PA-C · Stanford University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-02-13
Primary Completion
2022-05-01
Completion
2022-05-01

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03170778 on ClinicalTrials.gov