Hôpital BICHAT
Paris, 75018, France
NCT Number: NCT03452826
To assess the effectiveness of a management strategy combining a broad panel respiratory mPCR and an algorithm of early antibiotic de-escalation and discontinuation based on both the mPCR results and the procalcitonin (intervention) in severe CAP, as compared to a conventional strategy (control).
A multicentre, parallel-group, open-label, randomized controlled trial. The primary assessment criterion est the number of antibiotic-free days at 28 days
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Paris, 75018, France
Randomization is performed immediately after the inclusion.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Other names: Antibiotic therapy to be adapted according to the result of mPCR (device)
Time frame: Day 28
the number of antibiotic free days at D28, which corresponds to the number of days alive without any at Day 28.
Time frame: Day 28 and day 90
Mortality rate at D28 and D90
Time frame: Day 28
Number of defined daily dose (DDD) per 100 patient days of broad- and narrow-spectrum antibiotics
Time frame: Day 28
Antibiotics duration at D28
Time frame: Day 28
Number of organ-failure free days (based on SOFA) at D28
Time frame: Day 28
Incidence rates of bacterial superinfections at D28
Time frame: Day 28
Incidence rates of colonization/infection with multidrug resistant bacteria and Clostridium difficile infections at D28
Time frame: Day 28
Incidence rates of relapse (same pathogen) or reinfection (another pathogen) at D28
Time frame: Day 90
Duration of ICU and hospital stay
Time frame: Day 90
Cost of the total hospital admissions (including 90-day repeated admissions), ICU costs, cost of the microbiological diagnostic workup;
Time frame: Day 90
Incremental / decremental cost effectiveness ratio in cost per treatment success (90-day composite of all-cause death and infection recurrence).
Time frame: Day 28
Sensitivity, specificity, and likelihood ratios of the broad panel mPCR Film Array for the diagnosis of pneumonia, taking the conventional microbiological tests as reference
Time frame: Day 90
Euroquol questionary (EQ-5D-3L)
Time frame: Day 28
Sensitivity, specificity, and likelihood ratios of the broad panel mPCR Film Array for the diagnosis of ventilator associated pneumonia (in the intervention group only), taking the conventional microbiological tests as reference.
Assistance Publique - Hôpitaux de Paris
Other
Combined Use of a Respiratory Broad Panel MULTIplex PCR and Procalcitonin to Reduce Antibiotics Exposure in Patients With Severe Community-Acquired Pneumonia: a Multicentre, Parallel-group, Open-label, Randomized Controlled Trial.
Acronym: MULTI-CAP
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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