Perfusion Index in Anesthesia

Monitoring, Physiological Clinical Trial

Official title:

Peripheral Perfusion Index as Marker for Systemic Hemodynamics During Anesthesia

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02989441
• Other study ID #: H-16030081
• Status: Completed
• Start date: November 2016
• Est. completion date: June 2018

Study information

• Verified date: August 2018
• Source: Hvidovre University Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

In patients under general anesthesia the investigators wish to investigate association and covariance between a peripheral perfusion index as obtained by Radical 7 monitor (Masimo, Irvine, CA, USA) and more traditional hemodynamic parameters, ie. invasive blood pressure and SV as obtained by LiDCO rapid monitor (LiDCO Ldt., London, UK)

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: June 2018
• Est. primary completion date: March 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Patients for elective and sub-acute surgical repair of para-oesophagal hernia.

• Willingness to participate

Exclusion Criteria:

• Patient refusal

Related Conditions & MeSH terms

• Monitoring, Physiological

Locations

Country	Name	City	State
Denmark	Hvidovre University Hospital	Hvidovre	Capital Region

Sponsors (1)

Lead Sponsor	Collaborator
Jakob Højlund

Country where clinical trial is conducted

Denmark, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Co-variance between Perfusion Index (PI) and Cardiac Output (CO) and Stroke Volume (SV)		Intra-operative
Secondary	Co-variance between Perfusion Index (PI) and Mean Arterial Pressure (MAP)		Intra-operative