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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01037803
Other study ID # USILAN-1
Secondary ID
Status Completed
Phase N/A
First received December 21, 2009
Last updated January 17, 2011
Start date October 2008
Est. completion date December 2010

Study information

Verified date January 2011
Source Region Skane
Contact n/a
Is FDA regulated No
Health authority Sweden: The National Board of Health and Welfare
Study type Observational

Clinical Trial Summary

Does sublingual SDF-imaging results correlate with other haemodynamic parameters measured perioperatively and with postoperative morbidity/complications.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date December 2010
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 88 Years
Eligibility Inclusion:

- major surgery > 3h requiring arterial cannulation and central venous access

Exclusion Criteria:

- denied patient consent

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Sweden University of Lund and Lund University Hospital Lund Skane

Sponsors (1)

Lead Sponsor Collaborator
Region Skane

Country where clinical trial is conducted

Sweden, 

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