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NCT04620694 Clinical Trial

Impact of Arterial Cannulation Site on Vasopressor Requirement in Cardiac Surgery

Cardiac Disease Clinical Trial

— ATRAP-GCS  

Official title:
Impact of Arterial Cannulation Site on Vasopressor Requirement During Cardiac Surgery: a Monocentric Prospective Cohort Study

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04620694
Other study ID # 69HCL20_0947
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date October 1, 2020
Est. completion date February 2021

Study information
Verified date November 2020
Source Hospices Civils de Lyon
Contact Remi Schweizer, MD
Phone 0033472318933
Email remi.schweizer@chu-lyon.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Choice of arterial cannulation site during cardiac surgery is controversial. Some physicians in our institution prefer radial artery site, others prefer aortic site (via femoral artery or brachial artery). The investigators aim to compare these two strategies for vasopressor requirement. The study hypothesis is that radial artery cannulation is associated with a larger dose of vasopressor due aortic to radial arterial pressure gradient phenomenon.

Recruitment information / eligibility
Status Recruiting
Enrollment 350
Est. completion date February 2021
Est. primary completion date February 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adult patient - Scheduled for cardiac surgery with cardiopulmonary bypass Exclusion Criteria: - More than one arterial cannula at the beginning of the surgery

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Choice of arterial cannulation site at the beginning of the surgery
Choice of arterial cannulation site at the beginning of the surgery is at the discretion of the anesthesia physician.

Locations
Country Name City State
France Hôpital Louis Pradel Lyon

Sponsors (1)
Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Intraoperative vasopressor requirement Mean intraoperative dosage of Norepinephrine (µg.kg-1.min-1) end of surgery
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