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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04017182
Other study ID # 04072019
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date April 1, 2021
Est. completion date December 1, 2021

Study information

Verified date March 2021
Source Ramathibodi Hospital
Contact Thanist Pravitharangul, MD
Phone 66866633694
Email thnst_yu@msn.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

After installation of central venous catheter in patients under general anesthesia, paired sample of superior vena cava central venous blood and right external jugular venous blood will be collected and send to central laboratory for venous blood gas analysis. Correlation between superior vena cava central venous blood and right external jugular venous blood oxygen saturation will be determined as primary outcome.


Description:

All patients age between 18-65 year old who undergoing surgery under general anesthesia and superior vena cava central venous catheter installation anticipated are eligible. The tips of superior vena cava central venous catheter was confirmed by Chest x-ray. Next 1 hour after skin incision, 1 ml of venous blood sample is taken from superior vena cava central venous catheter of right external jugular vein then send to central laboratory for venous blood gas analysis. The demographic data will be recorded. Correlation between superior vena cava central venous blood and right external jugular venous blood oxygen saturation will be determined the primary outcome and partial pressure of carbon dioxide will be determined as a secondary outcome.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 40
Est. completion date December 1, 2021
Est. primary completion date December 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Written consent obtained from patient or next of kin a day before operation date - Patient age between 18-65 years old undergoing syrgery under general anesthesia - Superior vena cava central venous catheter anticipated for CVP mesurement, innotropic or vasopressor administration,pulmonary artery catheter insertion route - Anticipated right external jugular venous sampling time less than 5 minutes - The site of blood sample collection easily access during operation Exclusion Criteria: - No jugular central venous catheter installation or other route selected - Duration of paired sample collection more than 10 minutes - Can not collected blood sample from right external jugular vein within 3 attemps - The site of blood sample collection difficulty access during operation - Pateint or next of kin refuse to participate

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Thailand Department of Anesthesiology, Ramathibodi Hospital Bankok Bangkok

Sponsors (1)

Lead Sponsor Collaborator
Ramathibodi Hospital

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary Correlation of venous oxygen saturation Correlation of venous oxygen saturation between external jugular vein and superior vena cava 1 hour
Secondary Correlation of venous partial pressure of carbon dioxide Correlation of venous partial pressure of carbon dioxide between external jugular vein and superior vena cava 1 hour
Secondary Relationship between superior vena cava central venous and external jugular venous oxygen saturation Linear regression to determine prediction equation between superior vena cava oxygen saturation and external jugular vein oxygen saturation 1 hour