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Intrapulmonary pharmacokinetics study on inhalation of colistin sulfate in critically ill patients

Intrapulmonary pharmacokinetics study on inhalation of colistin sulfate in critically ill patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200055877
Enrollment
Unknown
Registered
2022-01-22
Start date
2022-01-22
Completion date
Unknown
Last updated
2023-07-02

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

Conditions

HAP/VAP

Interventions

treatment group:Colistin sulfate aerosol inhalation

Sponsors

Changxing People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. HAP/VAP patients with respiratory tract infection/colonization by multidrug-resistant bacteria, the pathogen susceptibility test is sensitive to colistin; 2. Aged 18 years and over, male or female.

Exclusion criteria

Exclusion criteria: 1.Patients who refuse to join the group, or patients who cannot obtain blood and bronchoalveolar lavage fluid samples due to the unwillingness of the patient and the patient's family; 2.Those who have unacceptable adverse reactions or serious adverse reactions; 3.Pregnant women and lactating women; 4.Patients who have received colistin within 7 days prior to inclusion, regardless of dose or route of administration; 5.Known allergy to colistin or polymyxin family products; 6.Personal and family history of muscle weakness; 7.HBV, HCV and HIV seropositive; 8.Patients with a history of severe bronchial asthma in the past.

Design outcomes

Primary

MeasureTime frame
Colistin concentration in miniBALF;

Countries

China

Contacts

Public ContactLin Bin

Changxing People's Hospital

lb_wzmc@126.com+86 572 6267652

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026