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 |
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Health condition(s) or Problem(s) studied | multidrug-resistant Pseudomonas aeruginosa infections in patients with hematological disease. |
Date of first enrollment | 2009/06/01 |
Target sample size | 5 |
Countries of recruitment | Japan |
Study type | Interventional |
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 Outcome | A clinical response at the end of colistin therapy |
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Secondary Outcome |
Key inclusion & exclusion criteria
Age minimum | Not applicable |
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Age maximum | Not applicable |
Gender | Male and Female |
Include criteria | |
Exclude criteria | 1. Allergy for colistin 2. A woman who is pregnant or has chance to be pregnant. |
Related Information
Primary Sponsor | University of Tokyo Hospital Department of Hamatology and Oncology |
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Secondary Sponsor | |
Source(s) of Monetary Support | None |
Secondary ID(s) |
Contact
public contact | |
Name | Fumihiko Nakamura |
Address | 7-3-1, Hongo, Bunkyo-ku, Tokyo, Japan Japan |
Telephone | 03-3815-5411 |
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 |
fnakamur-tky@umin.ac.jp | |
Affiliation | University of Tokyo Hospital hematology and Oncology |