UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000018083
Receipt number R000020841
Scientific Title Detection of sentinel lymph node metastases in endometrial cancer: Performance evaluation of the OSNA assay
Date of disclosure of the study information 2015/06/25
Last modified on 2024/01/04 09:08:30

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Basic information

Public title

Detection of sentinel lymph node metastases in endometrial cancer: Performance evaluation of the OSNA assay

Acronym

Performance evaluation of the OSNA assay

Scientific Title

Detection of sentinel lymph node metastases in endometrial cancer: Performance evaluation of the OSNA assay

Scientific Title:Acronym

Performance evaluation of the OSNA assay

Region

Japan


Condition

Condition

Endometrial cancer

Classification by specialty

Obstetrics and Gynecology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

Detection of sentinel lymph node metastases

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Concordance between the OSNA assay and histopathological examination

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

Diagnosis

Type of intervention

Device,equipment

Interventions/Control_1

Using OSNA assay, we perform the performance evaluation of sentinel lymph node metastatic diagnosis in 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

Endometrial cancer

Key exclusion criteria

1)lymph node metastasis and distant metastasis at their preoperative evaluation with magnetic resonance imaging(MRI) and/or computed tomography(CT)
2)history of treatment of radiotherapy and/or chemotherapy
3)history of treatment of uterine adnexectomy
4)an allergic medical history of RI and/or blue dye
5)ovarian metastasis and serosa invasion at their preoperative evaluation with MRI and/or CT.

Target sample size

240


Research contact person

Name of lead principal investigator

1st name Hideki
Middle name
Last name Tokunaga

Organization

Tohoku University Hospital

Division name

gynecology

Zip code

980-8574

Address

1-1 Seiryo-machi, Aoba-ku, Sendai

TEL

022-717-7254

Email

tokunagahideki@med.tohoku.ac.jp


Public contact

Name of contact person

1st name Satoshi
Middle name
Last name Okamoto

Organization

Tohoku University Hospital

Division name

gynecology

Zip code

980-8574

Address

1-1 Seiryo-machi, Aoba-ku, Sendai

TEL

022-717-7254

Homepage URL


Email

s-okamoto@med.tohoku.ac.jp


Sponsor or person

Institute

Tohoku University Hospital

Institute

Department

Personal name



Funding Source

Organization

Grant-in-Aid for Scientific Research

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

Tohoku University Hospital

Address

1-1 Seiryo-machi, Aoba-ku, Sendai

Tel

022-717-3964

Email

hosp-ken@bureau.tohoku.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



Other administrative information

Date of disclosure of the study information

2015 Year 06 Month 25 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

2015 Year 02 Month 04 Day

Date of IRB

2021 Year 02 Month 09 Day

Anticipated trial start date

2015 Year 02 Month 24 Day

Last follow-up date

2025 Year 02 Month 28 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2015 Year 06 Month 25 Day

Last modified on

2024 Year 01 Month 04 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000020841


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name