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Study identifier: NCT05280132 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Use of MULTIplex PCR, Procalcitonin, and Sputum Appearance to Reduce Duration of Antibiotic Therapy During Severe COPD EXAcerbation: A Controlled, Randomized, Open-label, Parallel-Group, Multicenter Trial

Condition: Acute Exacerbation of COPD  ·  Sponsor: Assistance Publique - Hôpitaux de Paris

PhaseNA
Planned participants204
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

COPD is a common chronic disease. Its natural course is characterized by Acute exacerbations (AE). This may require hospitalization or even ICU/RESUSCITATION admission. The most common causes are respiratory distress with hypercapnic acidosis that requires mechanical ventilation (Invasive or non-invasive). Lower respiratory tract infections, bacteria and/or viruses are the main pathogenic factors of AE. The treatment of AECOPD is initially symptomatic treatment, combining bronchodilators, ventilatory support (oxygen therapy and/or mechanical ventilation) and respiratory physiotherapy. Systemic corticosteroid therapy is optional. When i) the sputum is purulent and ii) increased dyspnea and / or an increase in sputum volume is observed, antibiotic treatment is recommended for hospitalized patients. Antibiotic therapy is routinely recommended when mechanical ventilation is required. During ICU/RESUSCITATION AECOPD, more than 85% of patients received antibiotic therapy, with a median duration of 8 to 9 days, and the benefit of antibiotic therapy is likely to be limited to infected patients. Suspected or documented lower respiratory tract bacteria, that is, 25% to 50% of patients. This will lead to overuse of antibiotics, which is a problem for patients and the community. A personalized antibiotic strategy could limit this phenomenon, relying on multimodal methods, using aspect of sputum (clinical method), procalcitonin (PCT) (biological method) and the FilmArray ™ Pneumonia Pan…

This description comes directly from the study's public registry record.

Talk to the study team

Guillaume VOIRIOT, Professor  ·  01 56 01 62 63  ·  guillaume.voiriot@aphp.fr

Muriel Fartoukh, PU-PH  ·  01 56 01 65 72  ·  muriel.fartoukh@aphp.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Intensive care department-Hospital TenonParis, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT05280132