UMIN-CTR Clinical Trial

Recruitment status Completed
Unique ID issued by UMIN UMIN000004181
Receipt No. R000005022
Official scientific title of the study Study of Robot-assisted Surgery for Gastric Tumor
Date of disclosure of the study information 2010/09/10
Last modified on 2017/01/20 (Ver. 9)

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Basic information
Official scientific title of the study Study of Robot-assisted Surgery for Gastric Tumor
Title of the study (Brief title) Study of Robot-assisted Surgery for Gastric Tumor
Region
Japan

Condition
Condition gastric tumors
Classification by specialty
Gastrointestinal surgery
Classification by malignancy Malignancy
Genomic information NO

Objectives
Narrative objectives1 assessment of feasibility and safety of robot-assisted gastric surgery
Basic objectives2 Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase Phase I

Assessment
Primary outcomes frequency of adverse events
Key secondary outcomes recurrence, prognosis

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 The use of robot-assisted surgical system for laparoscopic gastric surgery
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

Not applicable
Age-upper limit
80 years-old >=
Gender Male and Female
Key inclusion criteria (1) Patients with gastric tumors who is applicable for laparoscopic gastric surgery.
(2) Written informed consent is essential.
Key exclusion criteria (1)Woman in pregnancy or woman of child bearing potential and breast-feeding woman.
(2)Patients with psychiatric disease.
(3)Cases which the investigators think inadequate to this study.
Target sample size 10

Research contact person
Name of lead principal investigator Tetsu Nakamura
Organization Kobe University
Division name Department of Surgery
Address 7-5-2, Kusunoki-cho, Chuou-ku, Kobe, Japan
TEL 078-382-5925
Email tetsun@med.kobe-u.ac.jp

Public contact
Name of contact person Tetsu Nakamura
Organization Kobe University
Division name Department of Surgery
Address -5-2, Kusunoki-cho, Chuou-ku, Kobe, Japan
TEL 078-382-5925
Homepage URL
Email tetsun@med.kobe-u.ac.jp

Sponsor
Institute Kobe University
Institute
Department

Funding Source
Organization none
Organization
Division
Category of Funding Organization Self funding
Nationality of Funding Organization

Other related organizations
Co-sponsor
Name of secondary funder(s)

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
2010 Year 09 Month 10 Day

Progress
Recruitment status Completed
Date of protocol fixation
2010 Year 09 Month 09 Day
Anticipated trial start date
2011 Year 02 Month 01 Day
Last follow-up date
Date of closure to data entry
2017 Year 12 Month 31 Day
Date trial data considered complete
2017 Year 12 Month 31 Day
Date analysis concluded
2017 Year 12 Month 31 Day

Related information
URL releasing protocol
Publication of results Published
URL releasing results
Results
Other related information

Management information
Registered date
2010 Year 09 Month 09 Day
Last modified on
2017 Year 01 Month 20 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000005022