UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000006261
Receipt number R000007122
Scientific Title Analysis for the change of the intestinal bacterial flora by antimicrobials (antibiotics) with using T-RFLP method, and examination of the usefulness of probiotics for diarrhea caused by antimicrobials.
Date of disclosure of the study information 2011/09/01
Last modified on 2011/08/31 15:35:31

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Basic information

Public title

Analysis for the change of the intestinal bacterial flora by antimicrobials (antibiotics) with using T-RFLP method, and examination of the usefulness of probiotics for diarrhea caused by antimicrobials.

Acronym

Analysis for the change of the intestinal bacterial flora by antimicrobials (antibiotics) with using T-RFLP method, and examination of the usefulness of probiotics for diarrhea caused by antimicrobials.

Scientific Title

Analysis for the change of the intestinal bacterial flora by antimicrobials (antibiotics) with using T-RFLP method, and examination of the usefulness of probiotics for diarrhea caused by antimicrobials.

Scientific Title:Acronym

Analysis for the change of the intestinal bacterial flora by antimicrobials (antibiotics) with using T-RFLP method, and examination of the usefulness of probiotics for diarrhea caused by antimicrobials.

Region

Japan


Condition

Condition

Patients with nonsevere of acute pharyngitis, acute bronchitis, otitis media, etc. who need antimicrobials treatment.

Classification by specialty

Pediatrics

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To analyze the change of the intestinal bacterial flora by T-RFLP method for children treated by antimicrobials, and
to examine clinical usefulness of Bio-Three for diarrhea caused by antimicrobials by comparing with non-administration group as control.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Incidence of diarrhea

Key secondary outcomes

Analysis of the intestinal bacterial flora by T-RFLP method


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

No treatment

Stratification

NO

Dynamic allocation

NO

Institution consideration

Institution is not considered as adjustment factor.

Blocking

YES

Concealment

Numbered container method


Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

Probiotics administration group : Bio-Three powder or Bio-Tree tablets
6 months ~ less than 3 years : 0.5g t.i.d or 1 tablet t.i.d
3 years ~ less than 15 years : 1.0g t.i.d or 2 tablets t.i.d

Interventions/Control_2

Non probiotics administration group
(conventional therapy only)

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

6 months-old <=

Age-upper limit

180 months-old >

Gender

Male and Female

Key inclusion criteria

1.Patients with nonsevere of acute pharyngitis, acute bronchitis, otitis media, etc. who need antimicrobials treatment.
2.Patients whose representatives have submitted the letter of consent.
3.Patients who can observe this protocol.

Key exclusion criteria

1.Patients with diarrhea before administration.
2.Patients who received antimicrobials administration within one week before administration.
3.Patients with chronic, immunity system and serious diseases.
4.Patients who are applicable for chemotherapy, immunostimulation therapy, radiotherapy or surgery.
5.Patients with critical liver and kidney disorders and heart diseases, which may affect drug safety.
6.Patients with drug allergy.
7.Others; Patients who are judged as inappropriate for this test by lead principal investigator or contributing investigators.

Target sample size

120


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Toru Igarashi

Organization

Nippon Medical School Hospital

Division name

Department of Pediatric

Zip code


Address

1-1-5 Sendagi, Bunkyo-ku, Tokyo, Japan

TEL

03-3822-2131

Email



Public contact

Name of contact person

1st name
Middle name
Last name Toru Igarashi

Organization

Nippon Medical School Hospital

Division name

Department of Pediatrics

Zip code


Address

1-1-5 Sendagi, Bunkyo-ku, Tokyo, Japan

TEL

03-3822-2131

Homepage URL


Email

iga@nms.ac.jp


Sponsor or person

Institute

Nippon Medical School Hospital
Department of Pediatric

Institute

Department

Personal name



Funding Source

Organization

Toa Pharmaceutical Co., Ltd.

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization

Japan


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

2011 Year 09 Month 01 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

2011 Year 02 Month 18 Day

Date of IRB


Anticipated trial start date

2011 Year 08 Month 01 Day

Last follow-up date

2011 Year 11 Month 01 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2011 Year 08 Month 31 Day

Last modified on

2011 Year 08 Month 31 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000007122


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name