UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000008672
Receipt number R000010189
Scientific Title Safety and feasibility of capusule endoscopy for evaluation of small intestinal lesions of the scheduled liver transplant candidates
Date of disclosure of the study information 2012/08/10
Last modified on 2014/08/11 19:43:02

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Basic information

Public title

Safety and feasibility of capusule endoscopy for evaluation of small intestinal lesions of the scheduled liver transplant candidates

Acronym

Safety and feasibility of capusule endoscopy for scheduled liver transplant candidates

Scientific Title

Safety and feasibility of capusule endoscopy for evaluation of small intestinal lesions of the scheduled liver transplant candidates

Scientific Title:Acronym

Safety and feasibility of capusule endoscopy for scheduled liver transplant candidates

Region

Japan


Condition

Condition

scheduled liver transplant patients

Classification by specialty

Gastroenterology Hepato-biliary-pancreatic medicine Hepato-biliary-pancreatic surgery

Classification by malignancy

Others

Genomic information

YES


Objectives

Narrative objectives1

To examine safety and feasibility of the capsule endoscopy as the inspection in the preoperation for the liver transplant scheduled patients

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

lesions of small intestine of the liver transplant scheduled patients

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Diagnosis

Type of intervention

Device,equipment

Interventions/Control_1

capusule endoscopy

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

18 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

patients with scheduled of liver transplant in okayama university hospital

Key exclusion criteria

patients with possbility of retention of the capusule endoscopy

patients with impossible to swallow capusule endoscopy

Target sample size

30


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Seiji kawano

Organization

Okayama University Hospital

Division name

Department of endoscopy

Zip code


Address

2-5-1 shikatacho kitaku okayama city

TEL

086-235-7219

Email

skawano@mpd.biglobe.ne.jp


Public contact

Name of contact person

1st name
Middle name
Last name Seiji Kawano

Organization

Okayama University Hospital

Division name

Department of endoscopy

Zip code


Address

Shikatacho 2-5-1 kitaku Okayama city

TEL

086-235-7219

Homepage URL


Email

skawano@mpd.biglobe.ne.jp


Sponsor or person

Institute

Okayama University Hospital

Institute

Department

Personal name



Funding Source

Organization

Okayama University Hospital

Organization

Division

Category of Funding Organization

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

岡山大学病院


Other administrative information

Date of disclosure of the study information

2012 Year 08 Month 10 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

Enrolling by invitation

Date of protocol fixation

2012 Year 07 Month 25 Day

Date of IRB


Anticipated trial start date

2012 Year 07 Month 25 Day

Last follow-up date

2014 Year 12 Month 31 Day

Date of closure to data entry

2014 Year 12 Month 31 Day

Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2012 Year 08 Month 10 Day

Last modified on

2014 Year 08 Month 11 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000010189


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name