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2024-511896-13-00CompletedPhase 4

Use of MULTIplex PCR, procalcitonin and the appearance of sputum to reduce the duration of antibiotic therapy during severe COPD EXAcerbation: a trial controlled, randomized, open, in parallel groups, multicenter

Use of MULTIplex PCR, procalcitonin and the appearance of sputum to reduce the duration of antibiotic therapy during severe COPD EXAcerbation: a trial controlled, randomized, open, in parallel groups, multicenter (MULTI-EXA)

Source: EU CTIS (euclinicaltrials.eu) · Last updated 20 Mar 2026

Brief summary (registry, in English)

Evaluate the effectiveness in terms of antibiotic sparing of a personalized diagnostic and therapeutic strategy, compared to a usual strategy, during EA-COPD in the ICU/Rea.

Status (registry)
Completed
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
204 (actual)
First submitted
15 Oct 2024
Start date
9 Dec 2022
Lead sponsor
Assistance Publique Hopitaux De Paris
Diseases
COPD
EU CT number
2024-511896-13-00
EudraCT number
2021-005435-23

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 204
  • 13 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Antibiotic therapy formally indicated for a suspected or documented extra-respiratory infection
  • Congenital or acquired immunosuppression (congenital immune deficiency, progressive high-grade hematological malignancy, immunosuppressive drugs in the last 30 days including cytotoxic anti-cancer chemotherapy and anti-rejection drugs, corticosteroid therapy ≥ 20 mg/d of prednisone equivalent for at least 14 days, neutropenia, HIV with unknown or known CD4<200/µL in the last 6 months)

Other

  • Delay between admission to hospital and admission to ICU/ICU greater than 3 days
  • Current pregnancy.
  • Tracheotomy
  • Bronchial dilatation/cystic fibrosis
  • Moribund patient (imminent death)
  • Patient deprived of liberty and/or protected by law
  • Patient already included in MULTI-EXA
  • Patient already included in a type 1 interventional clinical study (RIPH1) relating to antibiotics

Who the study is looking for

  • Age ≥ 18 years old
  • Post-smoking COPD confirmed according to GOLD 2020, whatever the stage (I-IV)
  • Acute exacerbation (defined by the appearance or increase of one or more of the usual signs/symptoms of COPD) with acute respiratory failure requiring admission to the ICU/Resuscitation and mechanical ventilation (invasive or non-invasive or nasal oxygen therapy high flow rate with FiO2 ≥ 50%)
  • Consent (patient, relative or inclusion in emergency situation)
  • Affiliation to a social security scheme.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (13)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
University Hospital Of Clermont-Ferrand
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Clermont Ferrand Cedex 1FranceCompleted
Grand Hôpital de l'Est Francilien - Site de Marne la Vallée
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JOSSIGNYFranceCompleted
CHRU de Lille - Hôpital Salengro
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LilleFranceCompleted
Hospital Edouard Herriot
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Lyon Cedex 03FranceCompleted
Centre Hospital Region Metz Thionville
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Metz Cedex 03FranceCompleted
Centre Hospitalier Universitaire De Montpellier
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Montpellier Cedex 5FranceCompleted
Centre Hospitalier Universitaire de Nice
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NiceFranceCompleted
Hôpital Bichat - Claude-Bernard
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ParisFranceCompleted
Hôpital Saint-Antoine
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ParisFranceCompleted
Hopital Tenon
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Paris Cedex 20FranceCompleted
Centre Hospitalier Universitaire Reims
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Reims CedexFranceCompleted
Centre Hospitalier Universitaire Rouen
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Rouen CedexFranceCompleted
Hôpital d'Instructions des Armées Bégin
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Saint-MandéFranceCompleted

This page is information, not medical advice. Discuss any trial with your doctor.