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CompletedNCT04398381ProSyDICUUpdated May 28, 2020

Prognosis of SRD Patients in the ICU

An observational study in Systemic Rheumatic Diseases, Intensive Care Unit and Corticosteroids, sponsored by University Hospital, Montpellier. Completed at 1 site in France. Open to participants aged 18 Years to 100 Years. Per ClinicalTrials.gov, last updated 2020-05-28.

Sponsored by University Hospital, Montpellier · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
525
Ages
18 Years to 100 Years
Sex
All
01

Study summary

Critically ill systemic rheumatic disease (SRD) patients have benefited from better provision of rheumatic and critical care in recent years. Recent comprehensive data regarding in-hospital mortality and most importantly long-term outcome are scarce. The aim of this study is to assess short and long-term outcome of patients with SRD admitted to the ICU in a retrospective cohort study (2006 - 2016).

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Conditions studied

  • Systemic Rheumatic Diseases
  • Intensive Care Unit
  • Corticosteroids

Keywords

  • outcomes
  • prognostic factors
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In context

Rheumatic Diseases

377 studies on the registry are indexed under Rheumatic Diseases; 79 are open to participants now.

This study's enrollment of 525 is above the median of 245 across 157 observational studies indexed under Rheumatic Diseases.

Browse Rheumatic Diseases studies →

Lead sponsor

University Hospital, Montpellier is the lead sponsor of 1,244 studies on the registry; 225 are open to participants now.

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

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Who can participate

Ages eligible
18 Years to 100 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All consecutive SRD patients admitted to ICUs during the study period

Inclusion criteria

  • All consecutive SRD patients admitted to ICUs during the study period
  • at least one urine sample

Exclusion criteria

Exclusion criteria:

  • Age \< 18 years
  • Persons under protection
  • Paritcipation rejections
  • Admition to the ICU after scheduled surgery or trauma or suicide attempt unrelated to neurological involvement of SRD
  • Cancer treated with chemotherapy within a month before ICU admission
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Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
525 participants (actual)
Patient registry
No
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What researchers measure

Primary outcomes

  1. Mortality rate in the ICU associated risk factors

    Mortality rate in the ICU associated risk factors

    Time frame: 1 day

Secondary outcomes

  1. Mortality rate in the hospital and one-year after ICU admission and associated risk factors

    Mortality rate in the hospital and one-year after ICU admission and associated risk factors

    Time frame: 1 day

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Study locations

1 site
  • Uhmontpellier
    Montpellier, 34295, France
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References and documents

Individual participant data

Plan to share: Undecided — NC

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 28, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04398381
Lead sponsor
University Hospital, Montpellier
Collaborators
Groupe Hospitalier Pitie-Salpetriere, Sorbonne University, Hôpital Lariboisière Fernand Widal, Université Montpellier
Responsible party
Sponsor
First posted
May 21, 2020
Start date
Mar 1, 2017
Primary completion
Jun 1, 2019
Completion
Jun 30, 2019
Last update
May 28, 2020

Study contacts

Romaric Larcher, MD PhD
study director · UH Montpellier

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 May 2020. You cannot join it, but the record below documents what was studied.

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