UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000026155
Receipt number R000028352
Scientific Title Identification of sentinel lymph node with infrared fluorescence in lung cancer
Date of disclosure of the study information 2017/03/21
Last modified on 2017/02/15 22:58:24

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

Identification of sentinel lymph node with infrared fluorescence in lung cancer

Acronym

Identification of sentinel lymph node in lung cancer

Scientific Title

Identification of sentinel lymph node with infrared fluorescence in lung cancer

Scientific Title:Acronym

Identification of sentinel lymph node in lung cancer

Region

Japan


Condition

Condition

lung cancer

Classification by specialty

Chest surgery

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To identify sentinel lymph node and lymph flow in lung cancer, we will inject 0.5ml (5mg/ml) of ICG(Diagnogreen) to the normal lung parenchyma around clinical stage I lung cancer, and observate it by fluorescence endoscopic system. The identification rate of sentinel lymph node is analysed.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Primary endpoint is to assess sensitivity and specificity of sentinel lymph node identification. Standard operation for lung cancer (lobectomy and lymph node dissection) would be performed, and compare metastatic status of sentinel lymph node with that of the other mediastinal lymph node by postoperative histopathological examination.

Key secondary outcomes

To assess adverse effect for local injection of ICG.


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

Medicine

Interventions/Control_1

When we would reach thoracic cavity at usual lung cancer operation, we identify the location of tumors. we would inject 0.5ml of ICG to the normal lung parenchyma around tumor.Sentinel lymph node would be identified, to observe lymph node and lymph flow in lung cancer by fluorescence endoscopic system. Mediastinal lymph node dissection including this sentinel lymph node would be performed as usual as standard lung cancer surgery.
Postoperative histopathological examination showed the metastatic sentinel lymph node or not.

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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

primary lung cancer patient with clinical stage I according to preoperative examination.

Key exclusion criteria

The patient without tolerance for segmentectomy.

Target sample size

150


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Hiromitsu Takizawa

Organization

Institute of Biomedical Sciences, Tokushima University Graduate School

Division name

Department of Thoracic,Endocrine Surgery and Oncology

Zip code


Address

18-15, 3tyoume, Kuramototyo, Tokushima city, Tokushima prefecture

TEL

088-633-7143

Email

h-takizawa@mbf.ocn.ne.jp


Public contact

Name of contact person

1st name
Middle name
Last name Hiromitsu Takizawa

Organization

Institute of Biomedical Sciences, Tokushima University Graduate School

Division name

Department of Thoracic,Endocrine Surgery and Oncology

Zip code


Address

18-15, 3tyoume, Kuramototyo, Tokushima city, Tokushima prefecture

TEL

088-633-7143

Homepage URL


Email

h-takizawa@mbf.ocn.ne.jp


Sponsor or person

Institute

Institute of Biomedical Sciences, Tokushima University Graduate School

Institute

Department

Personal name



Funding Source

Organization

japan society for the promotion of science

Organization

Division

Category of Funding Organization

Government offices of other countries

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

2017 Year 03 Month 21 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

2017 Year 01 Month 01 Day

Date of IRB


Anticipated trial start date

2017 Year 04 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

2017 Year 02 Month 15 Day

Last modified on

2017 Year 02 Month 15 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000028352


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name