UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000012252
Receipt number R000014321
Scientific Title The evaluation for safety and usefulness of the robotic assisted surgery using the da Vinci Si Surgical System.
Date of disclosure of the study information 2013/11/08
Last modified on 2020/11/13 09:24:00

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Basic information

Public title

The evaluation for safety and usefulness of the robotic assisted surgery using the da Vinci Si Surgical System.

Acronym

The evaluation for safety and usefulness of the robotic assisted surgery for uterine cancer.

Scientific Title

The evaluation for safety and usefulness of the robotic assisted surgery using the da Vinci Si Surgical System.

Scientific Title:Acronym

The evaluation for safety and usefulness of the robotic assisted surgery for uterine cancer.

Region

Japan


Condition

Condition

Uterine corpus cancer

Classification by specialty

Obstetrics and Gynecology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study is the evaluation for safety usefulness of the robotic assisted surgery for uterine corpus cancer.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Operation time, blood loss, complications, postsurgical pain, the rate of conversions to open surgery, the duration of hospitalization

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Maneuver

Interventions/Control_1

Robotic assisted surgery ( total hysterectomy with bilateral salpingo-oophorectomy and pelvic lymphadenectomy)

Interventions/Control_2

Abdominal surgery ( total hysterectomy with bilateral salpingo-oophorectomy and pelvic lymphadenectomy)

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

80 years-old >

Gender

Female

Key inclusion criteria

uterine corpus cancer (endometrioid adenocarcinoma, FIGO IA and IB)

Key exclusion criteria

Inappropriate cases due to uterine cervical leiomyoma, severe obesity, severe intraabdominal adhesion and other factors

Target sample size

15


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Toru Fujioka

Organization

Ehime University Graduate School of Medicine

Division name

Obstetrics and Gynecology

Zip code


Address

Shitsukawa, Toon, Ehime, Japan

TEL

089-960-5379

Email

fujioka@m.ehime-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Toru Fujioka

Organization

Ehime University Graduate School of Medicine

Division name

Obstetrics and Gynecology

Zip code


Address

Shitsukawa, Toon, Ehime, Japan

TEL

089-960-5379

Homepage URL


Email

fujioka@m.ehime-u.ac.jp


Sponsor or person

Institute

Ehime University Graduate School of Medicine, Department of Obstetrics and Gynecology

Institute

Department

Personal name



Funding Source

Organization

Ehime University Hspital

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


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

2013 Year 11 Month 08 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

2013 Year 10 Month 21 Day

Date of IRB

2013 Year 10 Month 28 Day

Anticipated trial start date

2013 Year 11 Month 01 Day

Last follow-up date

2016 Year 10 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2013 Year 11 Month 08 Day

Last modified on

2020 Year 11 Month 13 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000014321


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name