Ataturk University
Erzurum, 25240, Turkey (Türkiye)
NCT Number: NCT07369206
This retrospective cohort study will evaluate whether syndromic clinical diagnoses present at ICU admission are associated with ICU mortality, independent of physiologic severity scores. Adult patients admitted to a tertiary mixed ICU during 2025 will be assessed.
Looking for future studies?
Notify Me18 year and older
All sexes
Observational
Erzurum, 25240, Turkey (Türkiye)
Data will be obtained retrospectively from the hospital information system and ICU clinical records. Variables will be recorded based on the first 24 hours after ICU admission. Demographics, admission characteristics, comorbidities, severity scores (APACHE II, SAPS, SOFA), and admission syndromic diagnoses (e.g., sepsis/septic shock, acute respiratory failure, ARDS, MODS) will be collected. The primary outcome is ICU mortality; secondary outcomes include ICU length of stay and ICU discharge disposition.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: From ICU admission until ICU discharge (end of index ICU stay), assessed up to 90 days
Death occurring during the index ICU stay (ICU mortality), abstracted from electronic medical records.
Time frame: From ICU admission to ICU discharge (index ICU stay), assessed at ICU discharge (up to 90 days)
ICU length of stay (days) during the index ICU admission, calculated as the difference between ICU admission and ICU discharge timestamps in the electronic medical record.
Time frame: At ICU discharge (index ICU stay; assessed at the time of ICU discharge in the medical record, up to 90 days)
Disposition at ICU discharge categorized as: death in ICU, transfer to hospital ward, or transfer to another facility; determined from the ICU discharge documentation in the electronic medical record.
Ataturk University
Other
Association of Admission Syndromic Diagnoses With ICU Mortality in a Mixed Adult Intensive Care Unit: Retrospective Cohort
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT03344627
Carbapenem, Clinical Outcome
Ratchathewi, Bangkok, Thailand
View Trial DetailsNCT07223684
Burn Injury, Burns
Tampa, Florida, United States
View Trial DetailsNCT07249762
Burn Injury, Burns
Tampa, Florida, United States
View Trial DetailsNCT05950984
Adult Children, Antibiotic Resistant Infection
London, United Kingdom
View Trial Details