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Status unknownNCT02290236Updated Oct 12, 2016

Monitored Saturation Post-ICU

An observational study in Sleep Apnea, Obstructive and Respiratory Insufficiency, sponsored by Karolinska University Hospital. Status unknown at 1 site in Sweden. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2016-10-12.

Sponsored by Karolinska University Hospital · Observational

The sponsor has not verified this record recently (last verified Oct 2016), so the status shown — last known as Enrolling by invitation — may be out of date.
Study type
Observational
Time perspective
Prospective
Enrollment
500
Ages
18 Years and older
Sex
All
01

Study 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.

02

Conditions studied

  • Sleep Apnea, Obstructive
  • Respiratory Insufficiency
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In context

Sleep Apnea Syndromes

2,162 studies on the registry are indexed under Sleep Apnea Syndromes; 290 are open to participants now.

This study's planned enrollment of 500 is above the median of 109 across 654 observational studies indexed under Sleep Apnea Syndromes.

Browse Sleep Apnea Syndromes studies →

Lead sponsor

Karolinska University Hospital is the lead sponsor of 275 studies on the registry; 54 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients that are discharged from the intensive care unit

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

Exclusion Criteria:

-

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Study design

Time perspective
Prospective
Enrollment
500 participants (estimated)
Patient registry
No

Interventions

  • DevicePulseoximetry

    Peripheral saturation will be recorded continuously

    Also known as: Saturation

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What researchers measure

Primary outcomes

  1. Oxygen desaturation index (ODI)

    Measured by continuous pulseoximetry

    Time frame: Days

Secondary outcomes

  1. STOP Bang screening questionnaire

    At inclusion the STOP BANG screening questionnaire will be completed

    Time frame: Days

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Study locations

1 site
  • Department of Anesthesiology, Surgical Services and Intensive Care Medicine, Karolinska University Hospital, Solna
    Stockholm, SE-17176, Sweden
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 12, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02290236
Lead sponsor
Karolinska University Hospital
Responsible party
Malin Jonsson Fagerlund (MD, PhD, Karolinska University Hospital) — Principal investigator
First posted
Nov 14, 2014
Start date
Sep 2014
Primary completion
Apr 2017 (estimated)
Completion
Jun 2017 (estimated)
Last update
Oct 12, 2016

Study contacts

Malin Jonsson Fagerlund, MD, PhD
principal investigator · Karolinska University Hospital and Karolinska Institutet

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2016. You cannot join it, but the record below documents what was studied.

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Discussion

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