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NCT02852889 Clinical Trial

Internal Jugular Vein Distensibility to Predict Fluid Responsiveness in Patients After Cardiac Surgery

Cardiac Surgery Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT02852889
Other study ID # B2016-077
Secondary ID
Status Recruiting
Phase N/A
First received July 29, 2016
Last updated August 3, 2016
Start date July 2016

Study information
Verified date August 2016
Source Shanghai Zhongshan Hospital
Contact Zhe Luo, PhD
Phone 021-64041990
Email luo.zhe@zs-hospital.sh.cn
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of the study was to verify the efficacy of using internal jugular vein (IJV) size and distensibility as an index of fluid responsiveness in mechanically ventilated patients after cardiac surgery.

Recruitment information / eligibility
Status Recruiting
Enrollment 50
Est. completion date
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- hypotension

- oliguria

- high lactate level

Exclusion Criteria:

- cardiac arrhythmia

- clinically relevant tricuspid or mitral regurgitation, clinically relevant right heart failure

- thrombosis in any large upper body veins

- bilaterally inserted venous catheters

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
China Zhongshan Hospital, Fudan University Shanghai Shanghai

Sponsors (1)
Lead Sponsor Collaborator
Shanghai Zhongshan Hospital

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary fluid responsiveness (mean artery pressure?cardiac output?stroke volume variation?internal jugular vein distensibility) CO increased more than 10% was defined as fluid responsiveness after fluid challenge (30min)
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