NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
UMIN ID: UMIN000002122

Registered date:26/06/2009

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

Basic Information

Recruitment status Complete: follow-up complete
Health condition(s) or Problem(s) studiedmultidrug-resistant Pseudomonas aeruginosa infections in patients with hematological disease.
Date of first enrollment2009/06/01
Target sample size5
Countries of recruitmentJapan
Study typeInterventional
Intervention(s)Colistin is administered intravenously. The dosage is 1.25-2.5mg/kg twice a day. The treetment period is between 3 and 28 days.

Outcome(s)

Primary OutcomeA clinical response at the end of colistin therapy
Secondary Outcome

Key inclusion & exclusion criteria

Age minimumNot applicable
Age maximumNot applicable
GenderMale and Female
Include criteria
Exclude criteria1. Allergy for colistin 2. A woman who is pregnant or has chance to be pregnant.

Related Information

Contact

public contact
Name Fumihiko Nakamura
Address 7-3-1, Hongo, Bunkyo-ku, Tokyo, Japan Japan
Telephone 03-3815-5411
E-mail fnakamur-tky@umin.ac.jp
Affiliation University of Tokyo Hospital Hematology and Oncology
scientific contact
Name Fumihiko Nakamura
Address 7-3-1, Hongo, Bunkyo-ku, Tokyo, Japan Japan
Telephone 03-3815-5411
E-mail fnakamur-tky@umin.ac.jp
Affiliation University of Tokyo Hospital hematology and Oncology