UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000023057
Receipt number R000026261
Scientific Title Feasibility and safety of robotic gastrectomy for gastric cancer using da Vinci Surgical System
Date of disclosure of the study information 2016/07/07
Last modified on 2019/07/30 09:15:29

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Basic information

Public title

Feasibility and safety of robotic gastrectomy for gastric cancer using da Vinci Surgical System

Acronym

Robotic Gastrectomy for gastric cancer

Scientific Title

Feasibility and safety of robotic gastrectomy for gastric cancer using da Vinci Surgical System

Scientific Title:Acronym

Robotic Gastrectomy for gastric cancer

Region

Japan


Condition

Condition

Gastric Cancer

Classification by specialty

Gastrointestinal surgery Adult

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To achieve the requirements for the institutes and operating surgeons of the "Senshiniryo" B study "Robotic Gastrectomy for Gastric Cancer"

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Morbidity (Clavien-Dindo Grade over IIIa)

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

NO

Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Maneuver

Interventions/Control_1

Robotic gastrectomy

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

85 years-old >=

Gender

Male and Female

Key inclusion criteria

1)Primary gastric adenocarcinoma pathorogically diagnosed with pap, tub1, tub2, por1, por2, sig, or muc.
2)clinical Stage I or II
3)Not meeting the indications for endoscopic resection
4) patient's own writtne informed concent is obtained.

Key exclusion criteria

1)Patients with a mental disorder who have difficulties in participating in the present study
2)preoperative therapy excluding non-curative endoscopic resection

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Hirofumi
Middle name
Last name Kawakubo

Organization

School of Medicien, Keio University

Division name

Department of Surgery

Zip code

160-8582

Address

35 Shinanomachi, Shinjyuku, Tokyo, 160-8582 Japan

TEL

03-3353-1211

Email

hkawakubo@z3.keio.jp


Public contact

Name of contact person

1st name Hirofumi
Middle name
Last name Kawakubo

Organization

School of Medicine, Keio University

Division name

Department of Surgery

Zip code

160-8582

Address

35 Shinanomachi, Shinjyuku, Tokyo, 160-8582 Japan

TEL

03-3353-1211

Homepage URL


Email

hkawakubo@z3.keio.jp


Sponsor or person

Institute

School of Medicine, Keio University

Institute

Department

Personal name



Funding Source

Organization

N/A

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

Keio University School of Medicine, Ethics Committee

Address

35 Shinanomachi, Shinjyuku, Tokyo, 160-8582 Japan

Tel

03-5363-3503

Email

med-rinri-jimu@adst.keio.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

慶應義塾大学病院(東京都)


Other administrative information

Date of disclosure of the study information

2016 Year 07 Month 07 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

Completed

Date of protocol fixation

2016 Year 05 Month 17 Day

Date of IRB

2018 Year 07 Month 07 Day

Anticipated trial start date

2018 Year 01 Month 17 Day

Last follow-up date

2018 Year 09 Month 09 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2016 Year 07 Month 07 Day

Last modified on

2019 Year 07 Month 30 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000026261


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name