UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000040067
Receipt number R000045686
Scientific Title Clinical evaluation of the efficacy and safety of robot-assisted hysterectomy using da Vinci surgical system for early endometrial cancer
Date of disclosure of the study information 2020/04/06
Last modified on 2021/04/15 09:11:50

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Basic information

Public title

Clinical evaluation of the efficacy and safety of robot-assisted hysterectomy using da Vinci surgical system for early endometrial cancer

Acronym

Clinical evaluation of the efficacy and safety of robot-assisted hysterectomy for early endometrial cancer

Scientific Title

Clinical evaluation of the efficacy and safety of robot-assisted hysterectomy using da Vinci surgical system for early endometrial cancer

Scientific Title:Acronym

Clinical evaluation of the efficacy and safety of robot-assisted hysterectomy for early endometrial cancer

Region

Japan


Condition

Condition

Endometrial cancer

Classification by specialty

Obstetrics and Gynecology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the efficacy and safety of robot-assisted hysterectomy using da Vinci surgical system for early endometrial cancer.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2


Developmental phase

Not applicable


Assessment

Primary outcomes

Incidence of intra- and post-operative complications

Key secondary outcomes

Anesthesia time, operative time, estimated blood loss, postoperative analgesic requirements, length of hospital stay, overall survival, progression free survival, sites of recurrence.


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 Maneuver

Interventions/Control_1

We perform robot-assisted hysterectomy using da Vinci surgical system for patients with early endometrial cancer.

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

75 years-old >=

Gender

Female

Key inclusion criteria

1. Patients with histologically diagnosed G1/G2 endometrioid carcinoma of uterine body.
2. Patients with clinical stage IA
3. Uterus is resectable with conventional laparoscopic surgery in size.
4. ECOG performance Status 0 or 1.
5. Informed written consent is obtained.

Key exclusion criteria

1. BMI is over 30.
2. Patients with severe complications.
3. History of multiple pelvic surgeries or severe pelvic endometriosis.
4. History of glaucoma.
5. History of cerebrovascular disease.
6. Patients who are judged to be inappropriate as subject to this study by the investigators.

Target sample size

10


Research contact person

Name of lead principal investigator

1st name haruko
Middle name
Last name Iwase

Organization

Kitasato University Hospital

Division name

Gynecology

Zip code

252-0375

Address

1-15-1, Kitasato, Minami-ku, Sagamihara city, Kanagawa

TEL

042-778-8414

Email

haiwase@med.kitasato-u.ac.jp


Public contact

Name of contact person

1st name Kento
Middle name
Last name Ohnishi

Organization

Kitasato University Hospital

Division name

Gynecology

Zip code

252-0375

Address

1-15-1, Kitasato, Minami-ku, Sagamihara city, Kanagawa

TEL

042-778-8414

Homepage URL


Email

kohnishi@med.kitasato-u.ac.jp


Sponsor or person

Institute

Kitasato University Hospital

Institute

Department

Personal name



Funding Source

Organization

Kitasato University Hospital

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

The Kitasato Institute Clinical Research Review Board

Address

1-15-1, Kitasato, Minami-ku, Sagamihara city, Kanagawa

Tel

042-778-8273

Email

rinrib@med.kitasato-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

北里大学病院


Other administrative information

Date of disclosure of the study information

2020 Year 04 Month 06 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

10

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

2020 Year 02 Month 12 Day

Date of IRB

2020 Year 04 Month 01 Day

Anticipated trial start date

2020 Year 05 Month 01 Day

Last follow-up date

2025 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2020 Year 04 Month 06 Day

Last modified on

2021 Year 04 Month 15 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000045686


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name