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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02859194
Other study ID # 4-2016-0124
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 31, 2016
Est. completion date October 14, 2016

Study information

Verified date July 2018
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

ECMO(Extracorporeal membrane oxygenation) is being essential for cardiopulmonary failure patients. There are two types of ECMO, which is veno-veno (V-V) that can be used in respiratory failure patients and veno-arterial (V-A) that can be used in cardiac failure patients. V-A ECMO can also be used during lung transplantation, substitution of cardiopulmonary bypass, which can show sufficient performance during operation and better postoperative outcome. However, regarding V-A ECMO circulating from femoral vein to femoral artery, there is a pro blem of differential hypoxia which might influence coronary artery and head vessels. In this prospective study, the investigators are planning to put another ECMO catheter into internal jugular vein which takes a role of left to right shunt, to mitigate the hypoxia of coronary artery.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date October 14, 2016
Est. primary completion date October 14, 2016
Accepts healthy volunteers No
Gender All
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

1. scheduled for double lung transplantation

Exclusion Criteria:

1. patients who have history of coronary artery occlusive disease

2. patients with arrhythmia

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Veno-veno-arterial ECMO


Locations

Country Name City State
Korea, Republic of Department of Anesthesiology and Pain Medicine, Anesthesia and Pain Research Institue, Yonsei Universiy College of Medicine Seoul

Sponsors (1)

Lead Sponsor Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary arterial blood oxygen partial pressure (PaO2) 5 min after jugular catheter flow 0ml/min
Primary arterial blood oxygen partial pressure (PaO2) 5 min after jugular catheter flow 500 ml/min
Primary arterial blood oxygen partial pressure (PaO2) 5 min after jugular catheter flow 1,000ml/min
Primary arterial blood oxygen partial pressure (PaO2) 5 min after jugular catheter flow 1,500ml/min
Secondary venous blood oxygen partial pressure (PvO2) 5 min after jugular catheter flow 0ml/min
Secondary venous blood oxygen partial pressure (PvO2) 5 min after jugular catheter flow 500 ml/min
Secondary venous blood oxygen partial pressure (PvO2) 5 min after jugular catheter flow 1,000ml/min
Secondary venous blood oxygen partial pressure (PvO2) 5 min after jugular catheter flow 1,500ml/min
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