Clinical trial Recruiting at 1 site Observational Ages 18 and up

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.

More Sepsis trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment760 (estimated)
SponsorHospital Israelita Albert Einstein
Academic / other
Locations1 site (Passo Fundo, Rio Grande do Sul)
StatusRecruiting
StartedJune 18, 2026
Main results expectedJune 2027
Study endsDecember 2027
Registry record updatedJuly 23, 2026
Trial IDNCT07502794 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

  • Hospital São Vicente de Paulo
    Passo Fundo, Rio Grande do Sul, Brazil
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.