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NCT02290236 Clinical Trial

Monitored Saturation Post-ICU

Sleep Apnea, Obstructive Clinical Trial

Official title:
Monitored Saturation Post-ICU; Correlation to Charted Saturation, Pre-intensive Care Unit Obstructive Sleep Apnea and Outcome

Clinical Trial Details — Status: Enrolling by invitation

Administrative data
NCT number NCT02290236
Other study ID # Post ICU Sat
Secondary ID
Status Enrolling by invitation
Phase N/A
First received October 6, 2014
Last updated October 11, 2016
Start date September 2014
Est. completion date June 2017

Study information
Verified date October 2016
Source Karolinska University Hospital
Contact n/a
Is FDA regulated No
Health authority Sweden: Regional Ethical Review Board
Study type Observational

Clinical Trial Summary

The overall aim with this project is to describe the correlation between measured and charted saturation after intensive care and also describe the saturation-pattern in these patients. The investigators will also correlate post-ICU desaturations measured as oxygen denaturation index and complications to pre-ICU obstructive sleep apnea and the STOP BANG screening questionnaire.

Recruitment information / eligibility
Status Enrolling by invitation
Enrollment 500
Est. completion date June 2017
Est. primary completion date April 2017
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- >18 years of age.

- Admitted to the Central Intensive Care Unit (CIVA)

- Signed informed conscent by the patient or a relative

Exclusion Criteria:

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

Intervention

Device:
• Pulseoximetry
Peripheral saturation will be recorded continuously

Locations
Country Name City State
Sweden Department of Anesthesiology, Surgical Services and Intensive Care Medicine, Karolinska University Hospital, Solna Stockholm

Sponsors (1)
Lead Sponsor Collaborator
Karolinska University Hospital

Country where clinical trial is conducted

Sweden, 

Outcome
Type Measure Description Time frame Safety issue
Primary Oxygen desaturation index (ODI) Measured by continuous pulseoximetry Days No
Secondary STOP Bang screening questionnaire At inclusion the STOP BANG screening questionnaire will be completed Days No
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