procalcitonin
Diagnostic Testblood test, measuring the concentration of PCT in ug/L
Other names: PCT
NCT Number: NCT05854901
This study the investigators will examine whether procalcitonin-guided treatment regarding antibiotic therapy is non-inferior to usual care in patients who are admitted because of an acute COPD exacerbation when it comes to treatment failure on day 30.
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Notify Me40 year and older
All sexes
Interventional
Not applicable
Zuyderland hospital, Heerlen, Limburg, Netherlands
Chronic obstructive pulmonary disease (COPD) is a prevalent disease, worldwide, and in the Netherlands with approximately 600.000 patients. COPD is currently the 3rd leading cause of death worldwide and is also a leading cause of disability-adjusted life years. Given the contribution of exacerbations both to loss in quality of life and to health-care costs, it is of paramount importance to improve the current treatment of exacerbations.
Pulmonary physicians are well aware of overuse of antibiotics, but lack the tools to decide which medication to give in the clinical setting. Biomarkers may aid towards a more personalized treatment of acute COPD exacerbations (AECOPD). Procalcitonin (PCT), the precursor of calcitonin, is released in response to a bacterial infection by many tissues within 6-12 hours after the onset of infection, while the concentration is only minimally raised in viral infections, making it a relative specific diagnostic tool for bacterial infection. Several trials have shown a reduction in antibiotic consumption in AECOPD when using a PCT-guided treatment algorithm. Recent systematic reviews concluded that appropriately powered trials are lacking to confirm that clinical outcomes are comparable with usual care.
In this study the investigators will examine whether a PCT-guided treatment regarding antibiotic therapy is non-inferior to usual care in patients who are admitted because of an acute COPD exacerbation when it comes to treatment failure on day 30.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
blood test, measuring the concentration of PCT in ug/L
Other names: PCT
The physician's decided whether the patient will receive antibiotic treatment or not
Time frame: 30 days
Treatment failure is defined as disease-related mortality, need for endotracheal intubation or vasopressors, renal failure (defined as Kidney Disease: Improving Global Outcomes (KDIGO) stage 3 - new renal replacement therapy, tripling of baseline creatinine, or serum creatinine > or = 350 umol/L), lung abcess/empyema, development of pneumonia or rehospitalization within 30 days after inclusion.
Time frame: change between baseline and after 30 days
Incomplete resolution of the clinical signs and symptoms associated with the AECOPD at day 30 after inclusion of the study (i.e. not reaching the baseline condition prior to the AECOPD) scored using the modified Anthonisen criteria
Time frame: day 30
Incomplete resolution of the clinical signs and symptoms associated with the AECOPD at day 30 after inclusion of the study (i.e. not reaching the baseline condition prior to the AECOPD) scored using the modified Anthonisen criteria
Time frame: baseline
Patients fill in the modified Anthonisen criteria card on day 1 as a baseline measure
Time frame: day 3
Patients fill in the modified Anthonisen criteria card on day 3
Time frame: day 5
Patients fill in the modified Anthonisen criteria card on day 1 as a baseline measure
Time frame: day 10
Patients fill in the modified Anthonisen criteria card on day 1 as a baseline measure
Time frame: 30 days
Decision to start antibiotic therapy after an initial opposite decision (after 48 hours)
Time frame: 30 days
Side effects of antibiotic treatment, such as gastro-intestinal complaints, allergic reactions
Time frame: 30 days
The cumulative amount of antibiotic treatment consumed by the patient during follow-up
Time frame: 30 days
The cumulative amount of prednisolone consumed by the patient during follow-up
Time frame: up to 30 days
Duration of time (in days) of the admission in hospital for the index exacerbation during follow-up
Time frame: 30 days
The presence of a new exacerbation, requiring treatment (prednisolone and/or antibiotic treatment) during follow-up
Time frame: change between baseline and after 30 days
PROM symptom score: EXACT - Respiratory symptoms scale
Time frame: baseline
PROM symptom score: EXACT - Respiratory symptoms scale
Time frame: day 10
PROM symptom score: EXACT - Respiratory symptoms scale
Time frame: day 30
PROM symptom score: EXACT - Respiratory symptoms scale
Time frame: baseline
COPD assessment test, quality of life questionnaire
Time frame: day 10
COPD assessment test, quality of life questionnaire
Time frame: day 30
COPD assessment test, quality of life questionnaire
Time frame: change between baseline and day 30
COPD assessment test, quality of life questionnaire
Time frame: baseline
quality of life questionnaire
Time frame: day 10
quality of life questionnaire
Time frame: day 30
quality of life questionnaire
Time frame: change between baseline and day 30
quality of life questionnaire
Time frame: 30 days
Medical consumption questionnaire, measuring the total amount of medical consumption (admission, ER visits, outpatient visits) during follow-up
Time frame: 30 days
Need for non-invasive ventilation after 72 hours of admission
Time frame: 30 days
· Time to complete resolution of symptoms according to daily symptom diaries evaluating the modified Anthonisen criteria
Time frame: On day 1 participants use a sputum color chart to report their current sputum color. This can be Mucoid, Mucopurulent (pale yellow/pale green), Purulent dark yellow, Purulent dark green
Sputum colour chart, as previously published by Murray MP et al. Murray MP, Sputum colour: a useful clinical tool in non-cystic fibrosis bronchiectasis. Eur Respir J. 2009 Aug;34(2):361-4. PMID 19648517.
Time frame: 30 days
Alongside the clinical trial, an economic evaluation will be performed conform the guidelines of the Health Care Institute Netherlands (17). This evaluation will be conducted from a societal and payer's perspective. When adopting the societal perspective, costs will include 30-day inpatient and outpatient (emergency room, specialist visits) hospital costs, primary care costs (visits to GP and nurse practitioner), medication costs, ambulance costs, productivity costs, informal care costs and travel costs.
Erasmus Medical Center
Other
Procalcitonin-guided Treatment Regarding Antibiotic Use for Acute COPD Exacerbations: a Prospective Randomised Controlled Trial
Acronym: PRECISION
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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