ClinicalTrials.gg
CompletedNCT03276650Still-ICUUpdated Sep 20, 2018

Admission of Adult-onset Still Disease Patients in the ICU

An observational study in Adult-Onset Still Disease and Critically Ill, sponsored by Central Hospital, Nancy, France. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2018-09-20.

Sponsored by Central Hospital, Nancy, France · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
45
Ages
18 Years and older
Sex
All
01

Study summary

Since its first description in 1971, diagnosing adult-onset Still's disease (AOSD), a rare multisystemic disorder considered as a multigenic autoinflammatory syndrome, remains challenging. Rarely, AOSD may present severe systemic manifestations and require intensive care. The main purpose of the Stil ICU study is to make the first description of the epidemiology of critically ill AOSD patients. The investigators will use a retrospective cohort study design with dual recruitment strategies: (1) via the AOSD referral centres network and (2) via a French academic medical ICU network.

02

Conditions studied

  • Adult-Onset Still Disease
  • Critically Ill
03

In context

Still's Disease, Adult-Onset

23 studies on the registry are indexed under Still's Disease, Adult-Onset; 5 are open to participants now.

This study's enrollment of 45 is below the median of 155 across 10 observational studies indexed under Still's Disease, Adult-Onset.

Browse Still's Disease, Adult-Onset studies →

Lead sponsor

Central Hospital, Nancy, France is the lead sponsor of 798 studies on the registry; 186 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adult AOSD patients admitted to ICU

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • AOSD (history of newly diagnosed)
  • ICU admission between January 2001 and June 2017

Exclusion criteria

Exclusion Criteria:

  • adults under protection
  • admission in step-down unit
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
45 participants (actual)
Patient registry
No

Groups and cohorts

  • critically ill AOSD patients

    no intervention Data collection from hospitalisation reports (administrative, biological, clinical, outcome)

    Other: data collection

Interventions

  • Otherdata collection

    biological, administrative, clinical, outcome date

06

What researchers measure

Primary outcomes

  1. number of patients

    Number of patients fulfilling the inclusion criteria

    Time frame: At inclusion

Secondary outcomes

  1. APACHE II

    Acute Physiologic Assessment and Chronic Health Evaluation II

    Time frame: 24hour after ICU admission

  2. Mortality

    Kaplan Meier

    Time frame: through study completion, maximum 17,5 years after admission

  3. Number of rehospitalisation in ICU

    need for critical care after the first hospitalisation in ICU

    Time frame: through study completion, maximum 17,5 years after admission

  4. number of hospitalisation in internal medicine ward

    number of hospitalisation in internal medicine ward after the first ICU stay

    Time frame: through study completion, maximum 17,5 years after admission

  5. recurrent relapses

    number of recurrent flares after the first hospitalisation in ICU

    Time frame: through study completion, maximum 17,5 years after admission

07

Study locations

1 site
  • CHRU
    Nancy, 54000, France
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Sep 2017 to primary completion in Jun 2018, 9 months.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 25, 2017
First posted
Sep 8, 2017
StartActual
Sep 1, 2017
Primary completionActual
Jun 1, 2018
CompletionActual
Aug 1, 2018
Last update
Sep 20, 2018
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 20, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03276650
Responsible party
Sponsor
First posted
Sep 8, 2017
Start date
Sep 1, 2017
Primary completion
Jun 1, 2018
Completion
Aug 1, 2018
Last update
Sep 20, 2018

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2018. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion