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NCT04398381 Clinical Trial

Prognosis of SRD Patients in the ICU

Intensive Care Unit Clinical Trial

— ProSyDICU  

Official title:
One-year Outcome of Critically Ill Patients With Systemic Rheumatic Disease: a Multicenter Cohort Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04398381
Other study ID # RECHMPL18_0289
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 1, 2017
Est. completion date June 30, 2019

Study information
Verified date May 2020
Source University Hospital, Montpellier
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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).

Recruitment information / eligibility
Status Completed
Enrollment 525
Est. completion date June 30, 2019
Est. primary completion date June 1, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion criteria:

- All consecutive SRD patients admitted to ICUs during the study period

- at least one urine sample

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

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
France Uhmontpellier Montpellier

Sponsors (5)
Lead Sponsor Collaborator
University Hospital, Montpellier Groupe Hospitalier Pitie-Salpetriere, Hôpital Lariboisière Fernand Widal, Sorbonne University, Université Montpellier

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Mortality rate in the ICU associated risk factors Mortality rate in the ICU associated risk factors 1 day
Secondary 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 1 day
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