UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000000851
Receipt number R000001021
Scientific Title Impact of comorbidities on the outcome of allogeneic hematopoietic stem cell transplantation
Date of disclosure of the study information 2007/11/01
Last modified on 2013/11/05 13:46:08

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Basic information

Public title

Impact of comorbidities on the outcome of allogeneic hematopoietic stem cell transplantation

Acronym

comorbidities on allo HCT

Scientific Title

Impact of comorbidities on the outcome of allogeneic hematopoietic stem cell transplantation

Scientific Title:Acronym

comorbidities on allo HCT

Region

Japan


Condition

Condition

hematologic diseases

Classification by specialty

Hematology and clinical oncology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

confirm the utility of HCT-CI in predicting non-relapse mortality and overall survival after HCT.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

non-relapse mortality and overall survival

Key secondary outcomes



Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


Interventions/Control_2


Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

20 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

all patients who receive HCT for the first time

Key exclusion criteria

patients who receive second HCT

Target sample size

600


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Shinichiro Okamoto

Organization

Keio University School of Medicine

Division name

Division of Hematology

Zip code


Address

35 Shinamomachi, Shinjyuku-ku, Tokyo

TEL

03-3353-1211

Email

okamoto@sc.itc.keio.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Aya Nakaya

Organization

Keio University School of Medicine

Division name

Division of Hematology

Zip code


Address

35 Shinamomachi, Shinjyuku-ku, Tokyo

TEL

03-3353-1211

Homepage URL


Email

nakaya1016@yahoo.co.jp


Sponsor or person

Institute

KSGCT

Institute

Department

Personal name



Funding Source

Organization

KSGCT

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2007 Year 11 Month 01 Day


Related information

URL releasing protocol


Publication of results

Published


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2007 Year 09 Month 01 Day

Date of IRB


Anticipated trial start date

2007 Year 09 Month 01 Day

Last follow-up date

2011 Year 09 Month 01 Day

Date of closure to data entry

2011 Year 09 Month 01 Day

Date trial data considered complete

2011 Year 09 Month 09 Day

Date analysis concluded

2012 Year 12 Month 01 Day


Other

Other related information

(1)calculate HCT-CI before HCT
(2)follow patients for 2 years after HCT
(3)confirm the utility of HCT-CI in predicting NRM and OS after HCT


Management information

Registered date

2007 Year 10 Month 15 Day

Last modified on

2013 Year 11 Month 05 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000001021


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name