UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000031195
Receipt number R000034893
Scientific Title Visualization of the urethra using a lighted urethral stent in operations for low rectal cancer
Date of disclosure of the study information 2018/03/01
Last modified on 2021/08/13 12:05:59

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Basic information

Public title

Visualization of the urethra using a lighted urethral stent in operations for low rectal cancer

Acronym

Visualization of the urethra using a lighted urethral stent in operations for low rectal cancer

Scientific Title

Visualization of the urethra using a lighted urethral stent in operations for low rectal cancer

Scientific Title:Acronym

Visualization of the urethra using a lighted urethral stent in operations for low rectal cancer

Region

Japan


Condition

Condition

low rectal cancer

Classification by specialty

Surgery in general Gastrointestinal surgery

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To investigate the usefulness of visualization of the urethra using a lighted stent in operations for low rectal cancer.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Others

Developmental phase



Assessment

Primary outcomes

Detection rate of the urethra

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

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

Lighted stent is placed into the urethra through urinary catheter during operation

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

Key inclusion criteria

Patients who have one of three surgical procedure: 1)Intersphincteric resection(ISR); 2)Abdominoperineal resection (APR); or 3)Total pelvic exenteration(TPE).

Key exclusion criteria

1)Rejection cases
2)Ineligible cases

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Obama
Middle name
Last name Kazutaka

Organization

Kyoto University Hospital

Division name

Surgery

Zip code

606-8507

Address

54, Shogoin, Kawahara-cho, Sakyo-ku, Kyoto

TEL

075-366-7595

Email

kobama@kuhp.kyoto-u.ac.jp


Public contact

Name of contact person

1st name Kenji
Middle name
Last name Kawada

Organization

Kyoto University Hospital

Division name

Surgery

Zip code

606-8507

Address

54, Shogoin, Kawahara-cho, Sakyo-ku, Kyoto

TEL

075-366-7595

Homepage URL


Email

kkawada@kuhp.kyoto-u.ac.jp


Sponsor or person

Institute

Kyoto University Hospital, Department of Surgery

Institute

Department

Personal name



Funding Source

Organization

Japan Society of Laparoscopic Colorectal Surgery

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

Kyoto University Graduate School and Faculty of Medicine, Ethics Committee

Address

Yoshida-Konoe-cho, Sakyo-ku, Kyoto

Tel

075-753-4680

Email

(e-mail) ethcom@kuhp.kyoto-u.ac.jp


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

2018 Year 03 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

No longer recruiting

Date of protocol fixation

2018 Year 02 Month 07 Day

Date of IRB

2018 Year 03 Month 28 Day

Anticipated trial start date

2018 Year 04 Month 01 Day

Last follow-up date

2022 Year 03 Month 27 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2018 Year 02 Month 07 Day

Last modified on

2021 Year 08 Month 13 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000034893


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name