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Procalcitonin-Guided Antibiotic Therapy in Bronchiectasis

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03058718
Enrollment
210
Registered
2017-02-23
Start date
2014-01-01
Completion date
2017-02-01
Last updated
2017-02-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Antibiotic Therapy, Bronchiectasis, Procalcitonin

Brief summary

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

Interventions

OTHERProcalcitonin

The application of antimicrobial agents is determined by PCT results.

OTHERClinical Experience

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

Sponsors

Qilu Hospital of Shandong University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Bronchiectasis was diagnosed by high-resolution computed tomography based on the criteria published by McShane PJ et al. 2. Acute exacerbations of bronchiectasis. 3. Aged \>= 18 years. 4. Procalcitonin been detected after admission.

Exclusion criteria

1. Associated with chronic obstructive pulmonary disease. 2. Associated with asthma. 3. Traction bronchiectasis caused by pulmonary fibrosis. 4. 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. 5. Clinical data were incomplete. 6. Can not follow up with the person.

Design outcomes

Primary

MeasureTime frame
Antimicrobial prescription rate14 days
Number of days of antimicrobial application14 days
The number of days in hospital14 days

Secondary

MeasureTime frame
Bacterial resistance rate14 days
The incidence of complications14 days
Effective rate of clinical treatment14 days
mortality rate14 days
The proportion of patients with at least once acute exacerbation in 6 months6 months
fungal infection rate14 days
Quality of life score6 months
Adverse reaction rate14 days

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026