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An exploratory study of administration of colistin for multidrug-resistant Pseudomonas aeruginosa infections in patients with hematological disease.

An exploratory study of administration of colistin for multidrug-resistant Pseudomonas aeruginosa infections in patients with hematological disease. - An exploratory study of administration of colistin for multidrug-resistant Pseudomonas aeruginosa infections in patients with hematological disease.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000002122
Enrollment
5
Registered
2009-06-26
Start date
2009-06-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

multidrug-resistant Pseudomonas aeruginosa infections in patients with hematological disease.

Interventions

Colistin is administered intravenously. The dosage is 1.25-2.5mg/kg twice a day. The treetment period is between 3 and 28 days.

Sponsors

University of Tokyo Hospital Department of Hamatology and Oncology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1 Patients with hematological disease. (Patients who received hematopoietic stem cell transplantation for non-hematological disease are included) 2 Multidrug-resistant Pseudomonas aeruginosa was detected by bacteria culture within one month 3 Patients with symptons due to Multidrug-resistant Pseudomonas aeruginosa infection 4 The patients who recieved intraveous antibiotic for more than three days within one week and the symptons of infection did not improve.

Exclusion criteria

Exclusion criteria: 1. Allergy for colistin 2. A woman who is pregnant or has chance to be pregnant.

Design outcomes

Primary

MeasureTime frame
A clinical response at the end of colistin therapy

Countries

Japan

Contacts

Public ContactFumihiko Nakamura

University of Tokyo Hospital Hematology and Oncology

fnakamur-tky@umin.ac.jp03-3815-5411

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026