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
Sites (13)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University Hospital Of Clermont-Ferrand Coordinator of this site? Confirm its status | Clermont Ferrand Cedex 1 | France | Completed |
| Grand Hôpital de l'Est Francilien - Site de Marne la Vallée Coordinator of this site? Confirm its status | JOSSIGNY | France | Completed |
| CHRU de Lille - Hôpital Salengro Coordinator of this site? Confirm its status | Lille | France | Completed |
| Hospital Edouard Herriot Coordinator of this site? Confirm its status | Lyon Cedex 03 | France | Completed |
| Centre Hospital Region Metz Thionville Coordinator of this site? Confirm its status | Metz Cedex 03 | France | Completed |
| Centre Hospitalier Universitaire De Montpellier Coordinator of this site? Confirm its status | Montpellier Cedex 5 | France | Completed |
| Centre Hospitalier Universitaire de Nice Coordinator of this site? Confirm its status | Nice | France | Completed |
| Hôpital Bichat - Claude-Bernard Coordinator of this site? Confirm its status | Paris | France | Completed |
| Hôpital Saint-Antoine Coordinator of this site? Confirm its status | Paris | France | Completed |
| Hopital Tenon Coordinator of this site? Confirm its status | Paris Cedex 20 | France | Completed |
| Centre Hospitalier Universitaire Reims Coordinator of this site? Confirm its status | Reims Cedex | France | Completed |
| Centre Hospitalier Universitaire Rouen Coordinator of this site? Confirm its status | Rouen Cedex | France | Completed |
| Hôpital d'Instructions des Armées Bégin Coordinator of this site? Confirm its status | Saint-Mandé | France | Completed |
This page is information, not medical advice. Discuss any trial with your doctor.