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Supplementary Oxygen in Surgical and Medical Wards Evaluated by 30-day Mortality

Supplementary Oxygen in Surgical and Medical Wards in the Capital Region of Denmark Evaluated by 30-day Mortality, a Retrospective Cohort Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03625700
Acronym
SOSAM
Enrollment
11196
Registered
2018-08-10
Start date
2014-01-01
Completion date
2020-12-31
Last updated
2021-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Oxygen Deficiency, Oxygen Toxicity

Brief summary

This study evaluates the use and effects of supplementary oxygen in surgical and medical wards on patients admitted to a hospital in the capital region of Denmark. The population will be divided in to three groups according to their oxygenation status. The main outcome will be 30-day mortality, with secondary outcomes being Length of stay, 30-day admission to ICU, 30-day reoperations, 30-day readmission, and peak values within 30-days of C-reactive protein, S-Creatinine, Troponin.

Interventions

Supplementary oxygen supplied via nasal catheter or oxygen mask during hospital admission.

Sponsors

Hannibal Troensegaard
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Admission date between 1st of January 2014 to 29th of December 2014 on a hospital in the capital region of Denmark * Age ≥18 * Unique (first) admission in database for either: * Hip fracture requiring surgery * Chronic obstructive pulmonary disease in exacerbation * Acute mycardial infarction * Open abdominal surgery

Exclusion criteria

* No data on saturation within 48 hours after * Admission (Medical patients) * Discharge from the post anaesthesia care unit (Surgical patients) * No data on primary outcome (30-day mortality)

Design outcomes

Primary

MeasureTime frameDescription
30- day mortality30 daysWill be reported as a fraction of positives within the exposure group population

Secondary

MeasureTime frameDescription
Length of stay30 daysLength of hospital stay in days
Organ markers in blood samples30 daysHighest value of C-reactive protein, Troponin and Creatinine within 30 days.
30- day admission to ICU30 daysWill be reported as a fraction of positives within the exposure group population.
30- day readmission30 dayswill be reported as a fraction of positives within the exposure group population.

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026