UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000001725
Receipt number R000002077
Scientific Title Mediastinal lymph node staging in lung cancer: A prospective comparison of CT/FDG-PET and EUS-FNA/EBUS-TBNA
Date of disclosure of the study information 2009/03/01
Last modified on 2010/08/25 08:10:38

* 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

Mediastinal lymph node staging in lung cancer: A prospective comparison of CT/FDG-PET and EUS-FNA/EBUS-TBNA

Acronym

Combined approach of EUS-FNA and EBUS-TBNA in mediastinal nodal staging of lung cancer

Scientific Title

Mediastinal lymph node staging in lung cancer: A prospective comparison of CT/FDG-PET and EUS-FNA/EBUS-TBNA

Scientific Title:Acronym

Combined approach of EUS-FNA and EBUS-TBNA in mediastinal nodal staging of lung cancer

Region

Japan


Condition

Condition

lung cancer

Classification by specialty

Pneumology Chest surgery

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To assess the feasibility of combined approach of EUS-FNA and EBUS-TBNA for N-stage in patients with lung cancer

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Phase II


Assessment

Primary outcomes

To compare the accuracy of CT/FDG-PET and EUS-FNA/EBUS-TBNA

Key secondary outcomes

Incidence of EUS-FNA/EBUS-TBNA related complications


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -but assessor(s) are blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Diagnosis

Type of intervention

Device,equipment Maneuver

Interventions/Control_1

CT, FDG-PET, EUS-FNA and EBUS-TBNA are performed in patients with lung 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


Not applicable

Gender

Male and Female

Key inclusion criteria

1.Patients with newly diagnosed or suspected lung cancer based on CT and bronchoscopic findings
2.The clinical stage is judged to be below T4, any N, M0 according to TNM subsets (UICC)
3.Patients obtained written informed consent

Key exclusion criteria

1.Patients with poor medical conditions of grade-4 and -5, according to ASA classification)
2.Patients with bleeding tendency and coagulopathy
3.Case in which the patient refused surgery

Target sample size

120


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Ichiro Yasuda

Organization

Gifu University Hospital

Division name

First Department of Internal Medicine

Zip code


Address

1-1 Yanagido, Gifu 501-1194

TEL

058-230-6308

Email



Public contact

Name of contact person

1st name
Middle name
Last name Ichiro Yasuda

Organization

Gifu University Hospital

Division name

First Department of Internal Medicine

Zip code


Address

1-1 Yanagido, 501-1194

TEL

058-230-6308

Homepage URL


Email

YASUDAIC@aol.com


Sponsor or person

Institute

First Department of Internal Medicine, Gifu University Hospital

Institute

Department

Personal name



Funding Source

Organization

None

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor

National Hospital Organization Nagara Medical Center

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

2009 Year 03 Month 01 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

2009 Year 02 Month 22 Day

Date of IRB


Anticipated trial start date

2009 Year 03 Month 01 Day

Last follow-up date

2010 Year 02 Month 01 Day

Date of closure to data entry

2010 Year 02 Month 01 Day

Date trial data considered complete

2010 Year 08 Month 01 Day

Date analysis concluded

2010 Year 08 Month 01 Day


Other

Other related information



Management information

Registered date

2009 Year 02 Month 22 Day

Last modified on

2010 Year 08 Month 25 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000002077


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name