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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03506191
Other study ID # RETROSTENO
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date January 1, 2017
Est. completion date September 30, 2018

Study information

Verified date July 2018
Source Groupe Hospitalier Pitie-Salpetriere
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Pneumonia is a major cause of ICU admission, or may complicate ICU course. Among the causative pathogens, Stenotrophomonas Maltophilia is a rare pathogen, but affects usually patients with chronic pulmonary co-morbidities, or with long duration of mechanical ventilation and multiples treatment with broad spectrum antimicrobial therapy. However, there are only a paucity of data regarding epidemiology, impact and outcome of Pneumonia due to Stenotrophomonas Maltophilia in critically ill patients.

Primary objective was to study factors associated with mortality in case of Pneumonia due to Stenotrophomonas Maltophilia. Secondary objectives were to describe factors associated with morbidity of Pneumonia due to Stenotrophomonas Maltophilia (duration of mechanical ventilation, ICU length of stay), and to report the characteristics of critically ill patients presenting Pneumonia due to Stenotrophomonas Maltophilia.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 300
Est. completion date September 30, 2018
Est. primary completion date July 30, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

Patients older than 18 years

Documented Stenotrophomonas maltophilia pneumonia:

- Clinical suspicion (= two criteria including: fever> 38.5°C, leukocytosis > 10^9/L or leukopenia < 4.10^8/L, purulent tracheobronchial secretions and a new or persistent infiltrate on chest radiography).

- Documented Stenotrophomonas maltophilia positive quantitative culture of a respiratory sample: bronchoalveolar lavage fluid (significant threshold, >10^4cfu/ml) or plugged telescopic catheter (significant threshold, >10^3cfu/ml) or quantitative endotracheal aspirate (significant threshold, >10^6cfu/ml).

Exclusion Criteria:

Study Design


Locations

Country Name City State
France Réanimation Polyvalente CHR Metz-Thionville Metz
France Department of Anesthesiology and Critical Care Medicine, University Hospital of NANCY Nancy
France Anesthesiology and Critical Care Medicine, Groupe Hospitalier Pitié-Salpêtrière Paris Ile-de-France
France Department of Anesthesiology and Critical Care Medicine, University Hospital of Strasbourg Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
Groupe Hospitalier Pitie-Salpetriere

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Treatment failure Treatment failure is defined as composite of death and recurrence of pneumonia due to Stenotrophomonas Maltophilia within 30 days of the first episode Day 30
Secondary Duration of mechanical ventilation Number of days under mechanical ventilation Day 30
Secondary Recurrence of pneumonia due to Stenotrophomonas Maltophilia New onset of pneumonia due to Stenotrophomonas Maltophilia Day 30
Secondary Mortality Day 30
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