UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000006535
Receipt number R000007741
Scientific Title Clinical study of Robot-assisted surgery using da Vinci S HD Surgical System for mediastinal tumors
Date of disclosure of the study information 2011/11/01
Last modified on 2016/10/20 09:02:44

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Basic information

Public title

Clinical study of Robot-assisted surgery using da Vinci S HD Surgical System for mediastinal tumors

Acronym

Clinical study of Robot-assisted surgery for mediastinal tumors

Scientific Title

Clinical study of Robot-assisted surgery using da Vinci S HD Surgical System for mediastinal tumors

Scientific Title:Acronym

Clinical study of Robot-assisted surgery for mediastinal tumors

Region

Japan


Condition

Condition

mediastinal diseases

Classification by specialty

Chest surgery

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To assess the usability and safety of endoscopic surgery using da Vinci S HD Surgical System for mediastinal diseases

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase



Assessment

Primary outcomes

Length of hospital stay

Key secondary outcomes

intra- and post-operative adverse events


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

Endoscopic surgery using da Vinci S HD Surgical System

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 and Female

Key inclusion criteria

1.Patients maintaining the functions of the main organs.
2.A case that an operation under the general anesthesia is possible.
3.A case that a document agrrement by the examination participation.

Key exclusion criteria

1.Pregnant or potentially women, nursing women
2.Past history of the open thoracotomy
3.Patients with psychiatric diseases
4.Patients with severe or complicated medical conditions, not allowing participation into this protocol

Target sample size

10


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Takamasa Onuki

Organization

Tokyo Women's Medical University of Medicine

Division name

Department of Surgery I

Zip code


Address

8-1 Kawada-cho, Shinjuku-ku, Tokyo

TEL

03-3353-8111

Email

tonuki@twmu.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Masato Kanzaki

Organization

Tokyo Women's Medical University of Medicine

Division name

Department of Surgery I

Zip code


Address

8-1 Kawada-cho

TEL

03-3353-8111

Homepage URL


Email

kanzaki@chi.twmu.ac.jp


Sponsor or person

Institute

Tokyo Women's Medical University of Medicine, Department of Surgery I

Institute

Department

Personal name



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)



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

2011 Year 11 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

Completed

Date of protocol fixation

2011 Year 08 Month 01 Day

Date of IRB


Anticipated trial start date

2011 Year 11 Month 01 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

2011 Year 10 Month 13 Day

Last modified on

2016 Year 10 Month 20 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000007741


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name