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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03052153
Other study ID # 2016H0435
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 17, 2017
Est. completion date February 4, 2021

Study information

Verified date September 2021
Source Ohio State University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study will evaluate if an association exists between levels of blood flow through the pulmonary veins and the incidence of graft dysfunction post operatively.


Description:

Lung transplantation surgery can be fraught with a multitude of early as well as delayed complications leading to increased morbidity and mortality. During lung transplant surgery, trans-esophageal echocardiography (TEE) is routinely used to identify cardiac anatomy and measure blood flow through the pulmonary veins. This blood flow is assessed both before and after the lung has been transplanted. Blood flow through these small caliber vessels can be impacted by many variables with a resulting reduction in blood circulating to the lung, although currently there is no agreement on an acceptable level of flow. This study will look at retrospective data from lung transplant surgeries undertaken at this institution since Jan 1st 2014 until November 18th 2016 with the goal of determining if an association exists between levels of blood flow through the pulmonary veins and the incidence of graft dysfunction post operatively.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date February 4, 2021
Est. primary completion date February 4, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. All adult patients = 18 years of age 2. Having undergone single or bilateral lung transplantation surgery at Ohio State University Wexner Medical Center between January 1st 2014 and November 18th 2016 Exclusion Criteria: 1. Patients = 18 years of age

Study Design


Related Conditions & MeSH terms


Intervention

Other:
No investigational intervention performed for this study
No investigational intervention for the purpose of this study was performed; data collected is retrospective data previously collected for non-research purposes.

Locations

Country Name City State
United States The Ohio State University Wexner Medical Center Columbus Ohio

Sponsors (1)

Lead Sponsor Collaborator
Ohio State University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary incidence of graft dysfunction To describe the relationship between intra-operative pulmonary vein systolic velocities and the incidence of graft dysfunction as defined by the International Society for Heart and Lung Transplantation (ISHLT). at 30 days post-transplant
Primary grade of graft dysfunction To describe the relationship between intra-operative pulmonary vein systolic velocities and grade of graft dysfunction as defined by the International Society for Heart and Lung Transplantation (ISHLT). at 30 days post-transplant
Secondary All-cause mortality To measure and report all-cause mortality at 30 days post-transplant. at 30 days post-transplant
Secondary Hospital Length of Stay To report subjects hospital length of stay for up to one year. From hospital admission to discharge up to one year.
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