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NCT Number: NCT07182916

Factors Associated With Early Readmission in Critical Care

The COVID-19 health crisis has highlighted pre-existing challenges in patient flow management within healthcare facilities, especially in critical care units. This has sparked debate regarding the sufficiency of critical care beds in France, while drawing attention to the lack of downstream structures. Inefficient patient flow, leading to bed occupancy bottlenecks, has been correlated with both critical care length of stay and morbidity. Unplanned early readmission to critical care further exacerbates these strains and prolongs hospital length of stay. Currently, no standardized criteria are available to guide safe discharge from critical care. A recent Delphi consensus study proposed a set of criteria, although largely subjective. The primary outcome of the present study is to identify factors associated with unplanned early readmission to critical care within 48 hours of discharge. Delayed discharge from critical care represents another major bottleneck contributing to system strain. The secondary outcome of this study is therefore to assess the proportion of critical care beds occupied by patients deemed ready for discharge by the medical team, as well as to analyze the reasons underlying such delayed transfers.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Hôpital Saint-Louis, AP-HP

Paris, 75010, France

Location status: Recruiting

Location contact

DEPRET FRANCOIS, MD

CONTACT

About this study

The COVID-19 health crisis has highlighted pre-existing challenges in patient flow management within healthcare facilities, especially in critical care units. This has sparked debate regarding the sufficiency of critical care beds in France, while drawing attention to the lack of downstream structures. Inefficient patient flow, leading to bed occupancy bottlenecks, has been correlated with both critical care length of stay and morbidity. Unplanned early readmission to critical care further exacerbates these strains and prolongs hospital length of stay. Currently, no standardized criteria are available to guide safe discharge from critical care. A recent Delphi consensus study proposed a set of criteria, although largely subjective. The primary outcome of the present study is to identify factors associated with unplanned early readmission to critical care within 48 hours of discharge. Delayed discharge from critical care represents another major bottleneck contributing to system strain. The secondary outcome of this study is therefore to assess the proportion of critical care beds occupied by patients deemed ready for discharge by the medical team, as well as to analyze the reasons underlying such delayed transfers.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients over 18 years of age
  • Hospitalized or admitted to the ICU

Exclusion criteria

  • Objection to the use of their data (by patient or a relative when applicable)
  • Patients under legal protection

Treatment and study plan

No intervention

Other

Only observation

Primary outcomes

  1. Early Readmission to the ICU

    Time frame: From the first day of recruitment to 48 hours after the end of recruitment

    Patients readmitted to the ICU less than 48 hours after their first discharge

Secondary outcomes

  1. Readmission to the ICU

    Time frame: From the first day of admission to 30 days of follow up

    Patients readmitted to the ICU less than 30 days after their first discharge

  2. 30-days mortality

    Time frame: From the first day of admission to 30 days of follow up

    Patients dead by day 30 of the follow-up

  3. Rate of bed occupancy by patients deemed fit for discharged

    Time frame: From the first day of the study to the 7th day of the study

    Patients still hospitalized in the ICU the day after they were deemed fit for discharge by the medical team

Study contacts

Contact information is provided by the study sponsor or research team.

François DEPRET

CONTACT

[email protected]

+33 1 42 49 93 94

Merlin DELOURME,, MD

CONTACT

[email protected]

+33 1 42 49 93 94

Sponsors and collaborators

Lead sponsor

Société Française d'Anesthésie et de Réanimation

Other

Registry information

Acronym: FRASC

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Sep 19, 2025
Registry last updated
May 29, 2026

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.