Long-term Outcomes After ICU Treatment for Sepsis
Official title: A Prospective Clinical Registry Assessing In-Hospital Management and Post-Discharge Outcomes Among Patients Hospitalized for Sepsis
Run by Hospital Israelita Albert Einstein · NCT07502794 · Data updated 2026-11-12
This study follows adults who were treated in ICUs for sepsis to see how they do during hospital stay and up to a year after discharge.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 760 (estimated) |
| Sponsor | Hospital Israelita Albert Einstein Academic / other |
| Locations | 1 site (Passo Fundo, Rio Grande do Sul) |
| Status | Recruiting |
| Started | June 18, 2026 |
| Main results expected | June 2027 |
| Study ends | December 2027 |
| Registry record updated | July 23, 2026 |
| Trial ID | NCT07502794 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults (18+) with a clinical diagnosis of sepsis or septic shock admitted to an ICU, able to provide or have a legal representative provide informed consent.
✕Probably not a fit
Patients who do not survive the initial hospitalization or who do not consent may not receive any direct benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a prospective, observational registry enrolling adults with sepsis admitted to ICUs. Data on clinical features, severity, and outcomes will be collected during hospitalization and at 3, 6, and 12 months post-discharge to describe short- and long-term health and mortality. The study is conducted in up to 30 ICUs in Brazil and uses standard care with no experimental interventions. It aims to identify factors associated with disease severity, hospital outcomes, and longer-term recovery. Enrollment requires informed consent and will target at least 760 participants aged 18 or older.
Why it matters
Potential benefit: The study could improve understanding of long-term recovery after sepsis, informing care planning and follow-up strategies.
How similar studies have gone: Observational registries in sepsis have provided valuable insights into long-term outcomes, supporting the feasibility of this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Clinical diagnosis of sepsis or septic shock during ICU hospitalization, according to the Sepsis-3 definition. * Age ≥18 years. * Written informed consent obtained from the participant or a legally authorized representative. Exclusion Criteria: * Limited prognosis with a life expectancy of less than 3 months due to conditions not related to sepsis. * Refusal to participate in the study
Where it's running
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Hospital São Vicente de Paulo
Passo Fundo, Rio Grande do Sul, Brazil Recruiting
Study contacts
- Study coordinator: Luciano C P Azevedo
- Email: luciano.azevedo@einsten.br
- Phone: 55+ 112151-1233
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.