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Target dose adjustment of busulfan in pediatric patients undergoing hematopoietic stem cell transplantation

Target dose adjustment of busulfan in pediatric patients undergoing hematopoietic stem cell transplantation - Target dose adjustment of busulfan in pediatric patients undergoing hematopoietic stem cell transplantation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000015166
Enrollment
50
Registered
2014-09-15
Start date
2013-05-07
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

hematological malignat disease, solid tumor, benign disease

Interventions

measurment of BU TDM

Sponsors

Nagoya University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The patient who is planed stem cell transplantation with BU as pre-conditioning

Exclusion criteria

Exclusion criteria: 1 uncontroled infection 2 uncontroled mental disease 3 pregnantor possible pregnant womanan

Design outcomes

Primary

MeasureTime frame
1 year survival after transplantation

Countries

Japan

Contacts

Public ContactYoshiyuki Takahashi

Nagoya University Graduate School of Medicine Department of Pediatrics

ytakaha@med.nagoya-u.ac.jp052-744-2294

Outcome results

None listed

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