NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
UMIN ID: UMIN000021015

Registered date:14/02/2016

Verifying the early diagnostic method of adenovirus-induced hemorrhagic cystitis after allogeneic hematopoietic stem cells transplantation

Basic Information

Recruitment status Complete: follow-up complete
Health condition(s) or Problem(s) studiedadenovirus-induced hemorrhagic cystitis after allogeneic hematopoietic stem cell transplantation
Date of first enrollment2016/02/15
Target sample size20
Countries of recruitmentJapan
Study typeInterventional
Intervention(s)Urinary adenoviral DNA is quantified in accordance with the schedule below. 1. Before the start of conditioning chemotherapy 2. Every two weeks after allogeneic hematopoietic stem cell transplantation 3. In case hemorrhagic cystitis has been developed, every week until improvement 4. At the outpatient clinic, once a month until one year post HSCT

Outcome(s)

Primary OutcomeThe efficacy of quantifying urinary adenoviral DNA for diagnosis of adenovirus-induced hemorrhagic cystitis
Secondary Outcome

Key inclusion & exclusion criteria

Age minimum16years-old
Age maximumNot applicable
GenderMale and Female
Include criteria
Exclude criteria1. Patients whom hemorrhagic cystitis has already developed 2. Patients who are recognized as inadaptable for this trial

Related Information

Contact

public contact
Name Yukio Kondo
Address 13-1, Takara-machi, Kanzawa, Ishikawa Japan
Telephone 076-234-2275
E-mail y-kondo@staff.kanazawa-u.ac.jp
Affiliation Kanazawa University Hospital Department of Hematology
scientific contact
Name Shinji Nakao
Address 13-1, Takara-machi, Kanzawa, Ishikawa Japan
Telephone 076-234-2275
E-mail snakao8205@staff.kanazawa-u.ac.jp
Affiliation Kanazawa University Hospital Department of Hematology