Skip to main content
OpenTrials
Completed

NCT Number: NCT05854901

PCT-guided Treatment Regarding Antibiotic Use for Acute COPD Exacerbations

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

40 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Zuyderland hospital, Heerlen, Limburg, Netherlands

Loading trial locations.

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • COPD, according to GOLD 2018 definition
  • Indication for hospitalization because of acute severe exacerbation of COPD, as defined by GOLD 2018 and modified Anthonisen criteria
  • Presence of at least 2 major symptoms of the modified Anthonisen criteria (acute deterioration in sputum volume, sputum purulence and dyspnea) or the presence of 1 major symptom and 1 minor symptom (coughing, wheeze, nasal discharge, sore throat, fever)
  • Post-bronchodilator FEV1/FVC < 0,70 and FEV1% < 80%pred. within last 5 years
  • At least 40 years
  • Smokers or ex-smokers with > 10 packyears
  • Written informed consent
  • Start of symptoms no more than 7 days before admission

Exclusion criteria

  • Indication for ICU and or non-invasive ventilation < 72h of admission
  • Pneumonia, radiologically confirmed
  • Infection at another site and/or sepsis according to the SIRS criteria (with tachycardia and tachypnea not being caused by the exacerbation)
  • COPD before age 40
  • Asthma, without presence of COPD.
  • Patients with COPD , with or without a history of asthma (in childhood or as an adolescent) will NOT be excluded/are allowed to participate.
  • Patients with Asthma/COPD overlap syndrome (with current asthma AND COPD) will NOT be excluded/are allowed to participate.
  • Clinically relevant heart failure or myocardial ischemia
  • Chronic use of immunosuppressants, including prednisolone (a prednisone equivalent of 10mg or less is allowed/is NOT an exclusion criterion)
  • Known bronchiectasis as a primary diagnosis
  • Colonisation with Pseudomonas spp. or other micro-organisms in recent cultures (last 60 days) not susceptible to amoxicillin-clavulanic acid
  • Pregnancy
  • Recent exacerbation (last 28 days)

Treatment and study plan

procalcitonin

Diagnostic Test

blood test, measuring the concentration of PCT in ug/L

Other names: PCT

Physician's decision

Other

The physician's decided whether the patient will receive antibiotic treatment or not

Primary outcomes

  1. Treatment failure

    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.

Secondary outcomes

  1. Incomplete resolution of the clinical signs and symptoms

    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

  2. Incomplete resolution of the clinical signs and symptoms

    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

  3. Modified Anthonisen criteria

    Time frame: baseline

    Patients fill in the modified Anthonisen criteria card on day 1 as a baseline measure

  4. Modified Anthonisen criteria

    Time frame: day 3

    Patients fill in the modified Anthonisen criteria card on day 3

  5. Modified Anthonisen criteria

    Time frame: day 5

    Patients fill in the modified Anthonisen criteria card on day 1 as a baseline measure

  6. Modified Anthonisen criteria

    Time frame: day 10

    Patients fill in the modified Anthonisen criteria card on day 1 as a baseline measure

  7. Decision to start antibiotic therapy after an initial opposite decision (after 48 hours)

    Time frame: 30 days

    Decision to start antibiotic therapy after an initial opposite decision (after 48 hours)

  8. Side effects of antibiotic treatment

    Time frame: 30 days

    Side effects of antibiotic treatment, such as gastro-intestinal complaints, allergic reactions

  9. Cumulative antibiotic consumption

    Time frame: 30 days

    The cumulative amount of antibiotic treatment consumed by the patient during follow-up

  10. Cumulative prednisolone consumption

    Time frame: 30 days

    The cumulative amount of prednisolone consumed by the patient during follow-up

  11. Length of hospitalization

    Time frame: up to 30 days

    Duration of time (in days) of the admission in hospital for the index exacerbation during follow-up

  12. Re-exacerbation

    Time frame: 30 days

    The presence of a new exacerbation, requiring treatment (prednisolone and/or antibiotic treatment) during follow-up

  13. EXACT respiratory questionnaire

    Time frame: change between baseline and after 30 days

    PROM symptom score: EXACT - Respiratory symptoms scale

  14. EXACT respiratory questionnaire

    Time frame: baseline

    PROM symptom score: EXACT - Respiratory symptoms scale

  15. EXACT respiratory questionnaire

    Time frame: day 10

    PROM symptom score: EXACT - Respiratory symptoms scale

  16. EXACT respiratory questionnaire

    Time frame: day 30

    PROM symptom score: EXACT - Respiratory symptoms scale

  17. CAT

    Time frame: baseline

    COPD assessment test, quality of life questionnaire

  18. CAT

    Time frame: day 10

    COPD assessment test, quality of life questionnaire

  19. CAT

    Time frame: day 30

    COPD assessment test, quality of life questionnaire

  20. CAT

    Time frame: change between baseline and day 30

    COPD assessment test, quality of life questionnaire

  21. EQ-5D-5L

    Time frame: baseline

    quality of life questionnaire

  22. EQ-5D-5L

    Time frame: day 10

    quality of life questionnaire

  23. EQ-5D-5L

    Time frame: day 30

    quality of life questionnaire

  24. EQ-5D-5L

    Time frame: change between baseline and day 30

    quality of life questionnaire

  25. iMCQ

    Time frame: 30 days

    Medical consumption questionnaire, measuring the total amount of medical consumption (admission, ER visits, outpatient visits) during follow-up

  26. Non-invasive ventilation after 72 hours of admission

    Time frame: 30 days

    Need for non-invasive ventilation after 72 hours of admission

  27. Time to complete resoluation of symptoms

    Time frame: 30 days

    · Time to complete resolution of symptoms according to daily symptom diaries evaluating the modified Anthonisen criteria

  28. Sputum Color Chart

    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.

Other outcomes

  1. Cost-effective analysis

    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.

Sponsors and collaborators

Lead sponsor

Erasmus Medical Center

Other

Collaborators

  • ZonMw: The Netherlands Organisation for Health Research and Development

Registry information

Official study title

Procalcitonin-guided Treatment Regarding Antibiotic Use for Acute COPD Exacerbations: a Prospective Randomised Controlled Trial

Acronym: PRECISION

Important dates

Study start
2021
Primary completion
2026
Study completion
2026
First posted
May 11, 2023
Registry last updated
Aug 13, 2026

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.

Published trials that share one or more normalized conditions with this study.