UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000029440
Receipt number R000033637
Scientific Title The study of probiotic supplementation for prophylaxis of infectious disorder including acute colitis in hematological malignancies
Date of disclosure of the study information 2017/10/06
Last modified on 2023/04/11 15:39:23

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Basic information

Public title

The study of probiotic supplementation for prophylaxis of infectious disorder including acute colitis in hematological malignancies

Acronym

Probiotic supplementation for prophylaxis
of infectious disorder in hematological malignancies

Scientific Title

The study of probiotic supplementation for prophylaxis of infectious disorder including acute colitis in hematological malignancies

Scientific Title:Acronym

Probiotic supplementation for prophylaxis
of infectious disorder in hematological malignancies

Region

Japan


Condition

Condition

Acute leukemia

Classification by specialty

Hematology and clinical oncology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To elucidate an efficacy of probiotics for prophylaxis of infection in hematological malignancies

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2


Developmental phase

Not applicable


Assessment

Primary outcomes

1)The frequencies or severity of gastrointestinal complication and febrile neutropenia
2)The frequencies or severity of bacterial colitis and sepsis

Key secondary outcomes

The effect of probiotics supplementation
in comparison with historical control


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Food

Interventions/Control_1

Intervention/Through-out of anti-cancer
treatment

Interventions/Control_2

Control group with no suppelementation

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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Tha cases of acute myeloid or lymphoid leukemia undergoing induction or consolidation chemotherapy

Key exclusion criteria

Nothing paticular

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Masao
Middle name
Last name Hagihara

Organization

Eiju General Hospital

Division name

Division of Hematology

Zip code

1108645

Address

2-23-16 Higashiueno Taito-ku Tokyo

TEL

0338338381

Email

hagihara@eijuhp.com


Public contact

Name of contact person

1st name Masao
Middle name
Last name Hagihara

Organization

Eiju General Hospital

Division name

Division of Hematology

Zip code

1108645

Address

2-23-16 Higashiueno Taito-ku Tokyo

TEL

0338338381

Homepage URL


Email

hagihara@eijuhp.com


Sponsor or person

Institute

Eiju General Hospital

Institute

Department

Personal name



Funding Source

Organization

Eiju General Hospital

Organization

Division

Category of Funding Organization

Non profit foundation

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Eiju General Hospital

Address

2-23-16,Higashi-Ueno,Taito-ku

Tel

81338338381

Email

hagihara@eijuhp.com


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

2017 Year 10 Month 06 Day


Related information

URL releasing protocol


Publication of results

Unpublished


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

Open public recruiting

Date of protocol fixation

2017 Year 03 Month 01 Day

Date of IRB

2017 Year 02 Month 22 Day

Anticipated trial start date

2017 Year 03 Month 01 Day

Last follow-up date

2023 Year 03 Month 31 Day

Date of closure to data entry

2023 Year 03 Month 31 Day

Date trial data considered complete


Date analysis concluded



Other

Other related information

Progress in analysis


Management information

Registered date

2017 Year 10 Month 05 Day

Last modified on

2023 Year 04 Month 11 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000033637


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name