A Comparison of Measurements of Peripheral Tissue Oxygenation by NONIN EQUANOX 7600, INVOS 5100c, and FORE-SIGHT

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Gorm Greisen, Rigshospitalet, Denmark
ClinicalTrials.gov Identifier:
NCT01552785
First received: March 6, 2012
Last updated: June 21, 2012
Last verified: June 2012

March 6, 2012
June 21, 2012
March 2012
May 2012   (final data collection date for primary outcome measure)
Absolute mean value of peripheral regional tissue oxygenation (rStO2) in percent [ Time Frame: 3 hours ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01552785 on ClinicalTrials.gov Archive Site
  • Reproducibility of measurement of peripheral regional tissue oxygenation (rStO2) in percent [ Time Frame: 3 hours ] [ Designated as safety issue: No ]
  • Sensitivity to changes in peripheral regional tissue oxygenation (rStO2) in percent [ Time Frame: 3 hours ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
A Comparison of Measurements of Peripheral Tissue Oxygenation by NONIN EQUANOX 7600, INVOS 5100c, and FORE-SIGHT
Not Provided

A comparison of three different devices using near infrared spectroscopy to measure the regional oxygenation. Both absolute values, reproducibility of measurements and sensitivity to changes will be estimated. The study hypothesis is that NONIN EQUANOX 7600 with sensor Model 8004CA, INVOS 5100c with sensor SAFB-SM and FORE-SIGHT with medium sensor have similar characteristics.

Not Provided
Observational
Observational Model: Case-Only
Time Perspective: Prospective
Not Provided
Not Provided
Non-Probability Sample

Citizens of Copenhagen

Near Infrared Spectroscopy
Device: Peripheral near infrared spectroscopy
Devices: NONIN 7600 EQUANOX with sensor Model 8004CA, INVOS 5100c with SAFB-SM, and FORE-SIGHT with medium sensor
Healthy adults
Intervention: Device: Peripheral near infrared spectroscopy
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
10
May 2012
May 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Adult
  • Double skin fold less than 1 cm on the lower arm

Exclusion Criteria:

  • Chronic diseases
Both
18 Years and older
Yes
Contact information is only displayed when the study is recruiting subjects
Denmark
 
NCT01552785
NIF010312
No
Gorm Greisen, Rigshospitalet, Denmark
Rigshospitalet, Denmark
Not Provided
Not Provided
Rigshospitalet, Denmark
June 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP