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OpenTrials
Completed

NCT Number: NCT03058718

Procalcitonin-Guided Antibiotic Therapy in Bronchiectasis

To explore effectiveness of procalcitonin-guided antibiotic therapy in acute exacerbations of bronchiectasis, and to explore the clinical value of procalcitonin in bronchiectasis.

Completed

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Key information

Age range

18 year–80 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Bronchiectasis was diagnosed by high-resolution computed tomography based on the criteria published by McShane PJ et al.
  • Acute exacerbations of bronchiectasis.
  • Aged >= 18 years.
  • Procalcitonin been detected after admission.

Exclusion criteria

  • Associated with chronic obstructive pulmonary disease.
  • Associated with asthma.
  • Traction bronchiectasis caused by pulmonary fibrosis.
  • Rule out other possible cause procalcitonin increased diseases such as cancer, connective tissue disease, active tuberculosis, chronic liver disease and respiratory system than the bacterial infection.
  • Clinical data were incomplete.
  • Can not follow up with the person.

Treatment and study plan

procalcitonin

Other

The application of antimicrobial agents is determined by PCT results.

Clinical Experience

Other

The application of antimicrobial agents is determined by clinical experience of doctors.

Primary outcomes

  1. Antimicrobial prescription rate

    Time frame: 14 days

  2. Number of days of antimicrobial application

    Time frame: 14 days

  3. The number of days in hospital

    Time frame: 14 days

Secondary outcomes

  1. Effective rate of clinical treatment

    Time frame: 14 days

  2. Quality of life score

    Time frame: 6 months

  3. Adverse reaction rate

    Time frame: 14 days

  4. Bacterial resistance rate

    Time frame: 14 days

  5. The incidence of complications

    Time frame: 14 days

  6. fungal infection rate

    Time frame: 14 days

  7. mortality rate

    Time frame: 14 days

  8. The proportion of patients with at least once acute exacerbation in 6 months

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

Qilu Hospital of Shandong University

Other

Registry information

Official study title

Effectiveness of Procalcitonin-Guided Antibiotic Therapy in Acute Exacerbations of Bronchiectasis: a Randomized Controlled Trial

Important dates

Study start
2014
Primary completion
2016
Study completion
2017
First posted
Feb 23, 2017
Registry last updated
Feb 23, 2017

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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