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Clinical Trials/NCT06727903
NCT06727903RecruitingNot Applicable

Development of a Predictive Model for Mortality in Patients Aged 75 or Older With Critical Illness

Consorci Sanitari de l'Alt Penedès i Garraf15 sites in 1 country450 target enrollmentStarted: March 20, 2025Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
450
Locations
15
Primary Endpoint
mortality
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The present study aims to develop a predictive model to identify elderly patients with the highest likelihood of mortality upon admission to an intensive care unit.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
75 Years to — (Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Men and women aged 75 or older.
  • •Admission to an ICU from the Emergency Department.
  • •Availability of or possibility to contact a participant's informant.
  • •Informed consent for participation in the study, either by the participant or a valid legal representative.

Exclusion Criteria

  • •Participants meeting any of the following exclusion criteria will not be included in the study:
  • •Patients transferred to the Emergency Department from a hospital ward.
  • •Patients who die within the first 24 hours of ICU admission.
  • •Patients admitted to Step-Down Units.
  • •Patients requiring ICU admission for any of the following reasons:
  • •Orotracheal intubation or advanced cardiopulmonary resuscitation performed prior to arrival at the Emergency Department.
  • •AV block awaiting pacemaker implantation. Activation of the STEMI or Stroke care pathway. Post-cardiac catheterization for acute coronary syndrome.
  • •Participation in another clinical study involving an intervention, procedure, or visit schedule that is incompatible with the present study.

Outcomes

Primary Outcomes

mortality

Time Frame: Day 90

mortality on day 90 from admission to Intensive Care Unit

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Consorci Sanitari de l'Alt Penedès i Garraf
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (15)

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