UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000006409
Receipt number R000007530
Scientific Title laparoscopic paraaortic lymphadenectomy for endometrial cancer
Date of disclosure of the study information 2011/09/27
Last modified on 2011/09/26 20:21:10

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Basic information

Public title

laparoscopic paraaortic lymphadenectomy for endometrial cancer

Acronym

laparoscopic paraaortic lymphadenectomy for endometrial cancer

Scientific Title

laparoscopic paraaortic lymphadenectomy for endometrial cancer

Scientific Title:Acronym

laparoscopic paraaortic lymphadenectomy for endometrial cancer

Region

Japan


Condition

Condition

endometrial cancer

Classification by specialty

Obstetrics and Gynecology Adult

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To confirm the safety and feasibility of laparoscopic paraaortic lymphadenectomy for endometrial cancer

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

complications concerning of the surgery and overall survival and disease free survival after 3 years

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


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Maneuver

Interventions/Control_1

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

20 years-old <=

Age-upper limit


Not applicable

Gender

Female

Key inclusion criteria

1) The patients who had diagnosed endometrial cancer by pathology, and expected stage 1-3 by MRI and CT.
2) 20 years old and elder
3) informed concent by signature
4) Who can be undergone general anesthesia

Key exclusion criteria

1) Who are diagnosed as not compatible for this test by phycological probleme
2) Who are diagnosed as not compatible for this test by the doctor in charge

Target sample size

10


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Ikuo Konishi

Organization

Dep. of Gynecology and Obstetrics, faculty of medecine,Kyoto univ.

Division name

Dep. of Gynecology and Obstetrics

Zip code


Address

54 Shogoin-Kawahara cho, Sakyo-ku, kyoto-city

TEL


Email



Public contact

Name of contact person

1st name
Middle name
Last name Kenzo Kosaka

Organization

Dep. of Gynecology and Obstetrics, faculty of medecine,Kyoto univ.

Division name

Dep. of Gynecology and Obstetrics

Zip code


Address


TEL

075-751-3269

Homepage URL


Email



Sponsor or person

Institute

Dep. of Gynecology and Obstetrics, faculty of medecine,Kyoto univ.

Institute

Department

Personal name



Funding Source

Organization

Kyoto university hospital

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 09 Month 27 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

Preinitiation

Date of protocol fixation

2011 Year 09 Month 12 Day

Date of IRB


Anticipated trial start date

2011 Year 09 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 09 Month 26 Day

Last modified on

2011 Year 09 Month 26 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000007530