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Active, not recruiting Observational

Study of the Characteristics of Acute Mycoplasma Resuscitation: ECRAN-PLASMA Study

NCT07479355 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2024-09-15
Last updated
2026-03-18

Condition(s) studied

Pneumonia

Investigational drug(s) / intervention(s)

Infectious disease epidemiology

Infectious disease epidemiology: evaluation of patient management, prognosis, and macrolide resistance rates in severe Mycoplasma pneumoniae and Chlamydia pneumoniae infections.

Study summary

The ECRAN-PLASMA study aims to analyze the characteristics of patients with Mycoplasma pneumoniae or Chlamydia pneumoniae pneumonia hospitalized in intensive care units (ICU), continuous monitoring units (USC), or intensive pulmonary care units (USIP). It evaluates their management, prognosis, and macrolide resistance rates.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Screening of all patients hospitalized in Intermediate Care Units (USC), Intensive Respiratory Care Units (USIP), and Intensive Care Units (ICU) * Inclusion of patients who test positive for Mycoplasma pneumoniae or Chlamydia pneumoniae Exclusion Criteria: * Patients under 18 years old

Primary outcome measure(s)

  • Incidence of Severe Mycoplasma pneumoniae and Chlamydia pneumoniae Infections — From hospital admission to hospital discharge (up to 60 days)
    Number of patients hospitalized in ICU, USC, or USIP with a confirmed diagnosis of Mycoplasma pneumoniae or Chlamydia pneumoniae.

Trial sites (1)

FacilityCityRegionStatus
Medecine intensive-reanimation Le Kremlin-Bicêtre France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07479355 on ClinicalTrials.gov ↗ ← All trials in France