UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000020713
Receipt number R000023642
Scientific Title The antispasmodic effective of shakuyaku-kanzo-to(TJ-68) on the colonic wall by direct spraying:a randomized controlled prospective study
Date of disclosure of the study information 2016/01/25
Last modified on 2017/07/26 11:48:51

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Basic information

Public title

The antispasmodic effective of shakuyaku-kanzo-to(TJ-68) on the colonic wall by direct spraying:a randomized controlled prospective study

Acronym

Shakuyaku-kanzo-to(TJ-68) for the colonoscopy

Scientific Title

The antispasmodic effective of shakuyaku-kanzo-to(TJ-68) on the colonic wall by direct spraying:a randomized controlled prospective study

Scientific Title:Acronym

Shakuyaku-kanzo-to(TJ-68) for the colonoscopy

Region

Japan


Condition

Condition

The over twenty years old patient perform the large intestine endoscopy

Classification by specialty

Gastroenterology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To estimate the prevention of colonic spasm when spraying the shakuyaku-kannzoutou in the large intestine

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The efficacy of the prevention of colonic spasm when spraying the shakuyaku-kannzoutou in the large intestine after three minute late

Key secondary outcomes

The background of patient and the time of the prevention of colonic spasm when spraying the shakuyaku-kannzoutou in the large intestine


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Placebo

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

shakuyaku-kanzoutou 5.0g in the 50ml saline of 36celsius

Interventions/Control_2

the 50ml saline of 36celsius

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

the pacient of performed the colonoscopy

Key exclusion criteria

the pacient has the allergy of shakuyaku-kannzoutou.
the pacient has the aldosteronism.
the pacient has the myopathy.
the pacient has the hypokalemia.
the pacient of post operation.
tha pacient has IBD.

Target sample size

70


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Kazuki okamoto

Organization

Kinki University School of Medicine

Division name

Department of gastroenterology and Hepatology

Zip code


Address

377-2onohigashi osakasayama-shi osaka-hu

TEL

072-366-0221

Email

kazukiokamoto815@yahoo.co.jp


Public contact

Name of contact person

1st name
Middle name
Last name Kimiko Yuge

Organization

Kinki University School of Medicine

Division name

Department of gastroenterology and Hepatology

Zip code


Address

377-2onohigashi osakasayama-shi osaka-hu

TEL

072-366-0221

Homepage URL


Email

kin-live@med.kindai.ac.jp


Sponsor or person

Institute

Kinki University School of Medicine,Department of gastroenterology and Hepatology

Institute

Department

Personal name



Funding Source

Organization

None

Organization

Division

Category of Funding Organization

Other

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

2016 Year 01 Month 25 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

Terminated

Date of protocol fixation

2016 Year 01 Month 23 Day

Date of IRB


Anticipated trial start date

2016 Year 03 Month 15 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2016 Year 01 Month 23 Day

Last modified on

2017 Year 07 Month 26 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000023642


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name