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NCT Number: NCT06612476

Interleukin 6-guided Antibiotic Prescriptions in AECOPD Inpatients

In this multicenter, prospective, randomized controlled study, we aimed to figure out, compared with the global chronic obstructive pulmonary disease initiative (GOLD) guideline -guided antibiotic therapy, whether Interleukin 6 (IL6)-guided antibiotic therapy for acute exacerbation of chronic obstructive pulmonary disease (AECOPD) can lead to a reduction in the use of antibiotics without increasing the rate of treatment failure.

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Key information

About this study

Acute exacerbation is the first leading cause of hospitalization and mortality among patients with COPD. Infection of bacteria has been detected in 49.59% of patients with AECOPD. Antibiotic prescriptions for AECOPD patients are usually based on GOLD guideline. However, the newest study reported that more than 85% of AECOPD inpatients received antibiotic prescription in the United States, Europe and China. Not all patients will equally experience benefit from antibiotics. Interleukin 6 (IL6) was determined as a reliable clinical biomarker in guiding antimicrobial use. It remains unclear whether IL6-guided antibiotic therapy is safe and effective for hospitalized patients with AECOPD.

The study will recruit 440 AECOPD inpatients from at least six hospitals based in China. Eligible participants will be assigned to receive either IL6-guided antibiotic therapy or GOLD-guided antibiotic therapy in 1:1 ratio randomly. The hypothesis for this study is that IL-6 guided antibiotic therapy will reduce the rate of antibiotic prescriptions for AECOPD without increasing the rate of treatment failure, compared with the group treated with GOLD-guided antibiotic therapy.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • AECOPD patients admitted to hospitals
  • The exacerbation has lasted for at least 24 hours but equal to or less than 21 days
  • ≥40 years of age but no more than 80 years old
  • With at least 10 pack-year history of smoking
  • Able to provide written informed consent and ensure the completion of the trial

Exclusion criteria

  • Axillary temperature≥38°C
  • Acute pneumonia identified by X-Ray or CT of the chest
  • Severe respiratory failure requiring admittance to ICU
  • Comorbidities require antibiotic therapy (i.e. infection at another site, systematic infection, active chronic inflammatory condition, specific viral infection)
  • Immunosuppression status (i.e., patients with HIV infection, with malignant tumor of blood system, receiving chemotherapy)
  • Concurrent diseases requiring corticosteroids (equivalent to 60mg prednisone/day or more than 30 days)
  • Antibiotic use in the previous four weeks
  • Current tracheotomy status
  • Bronchiectasis of origin other than COPD
  • Invasive mechanical ventilation
  • Patients diagnosed malignant tumors
  • Pregnant or lactating women, or women of childbearing age not using an acceptable method of contraception.
  • Newly diagnosed pulmonary embolism
  • Participation in another clinical trial

Treatment and study plan

Interleukin 6-guided antibiotic therapy

Drug

In Interleukin-6 group, antibiotic prescription decisions will made according to the results of IL-6.

GOLD-guided antibiotic therapy

Drug

In guideline group, antibiotic prescription decisions will made according to the recommendations of GOLD guideline.

Primary outcomes

  1. Incidence of antibiotic use

    Time frame: During the 30-day period after randomization

    Ratio of AECOPD patients given antibiotics

  2. Proportion of successful treatments

    Time frame: During the 30-day period after randomization

    Treatment success is achieved when there is a cure (full resolution of all symptoms and signs of the exacerbation) or improvement (diminishment or resolution of symptoms and signs from the exacerbation, with no additional symptoms or signs).

Secondary outcomes

  1. Incidence of antibiotic use

    Time frame: During the first day period after randomization

    Ratio of AECOPD patients given antibiotics

  2. Antibiotic utilization in the hospital

    Time frame: Between randomization and discharge, limited to 30 days

    Duration of antibiotic consumption for AECOPD and the percentage of patients treated with antibiotics for AECOPD from randomization to hospital discharge

  3. Duration of hospitalization

    Time frame: Between randomization and discharge, limited to 30 days

    Total days of hospitalization until study completion, averaging 30 days

  4. Frequency of subsequent exacerbations

    Time frame: During the 30-day period after randomization

    Ratio of patients who develop a subsequent acute exacerbation following recovery

  5. Incidence of hospital readmission

    Time frame: Between the discharge date and 30 days post-randomization

    Ratio of patients rehospitalized for AECOPD following discharge

  6. All-cause mortality

    Time frame: During the 30-day period after randomization

    Death due to any cause

  7. Frequency of ICU admissions

    Time frame: During the 30-day period after randomization

    Ratio of patients admitted to the intensive care unit

  8. noninvasive mechanical ventilation

    Time frame: During the 30-day period after randomization

    Ratio of patients provided with non-invasive mechanical ventilation

  9. Change in COPD assessment test

    Time frame: From the initial hospital admission baseline to 30 days after randomization

    The variation from the baseline at hospital admission to 30 days after randomization

  10. Change in St. George's Respiratory Questionnaire

    Time frame: From the initial hospital admission baseline to 30 days after randomization

    The variation from the baseline at hospital admission to 30 days after randomization

  11. Change in modified Medical Research Council (mMRC) score

    Time frame: From the initial hospital admission baseline to 30 days after randomization

    The variation from the baseline at hospital admission to 30 days after randomization

  12. Change in Hospital Anxiety and Depression Scale

    Time frame: From the initial hospital admission baseline to 30 days after randomization

    The variation from the baseline at hospital admission to 30 days after randomization

Study contacts

Contact information is provided by the study sponsor or research team.

Sponsors and collaborators

Lead sponsor

Ningbo No. 1 Hospital

Other

Registry information

Official study title

Interleukin 6-guided Antibiotic Prescriptions in AECOPD Inpatients: a Multicenter Randomized Controlled Trial

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Sep 25, 2024
Registry last updated
Sep 25, 2024

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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