UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000011871
Receipt number R000013875
Scientific Title The study of method to identify functional lymph vessels by contrast-enhanced ultrasonography in patients with lymphedema.
Date of disclosure of the study information 2013/10/01
Last modified on 2020/01/21 13:12:31

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Basic information

Public title

The study of method to identify functional lymph vessels by contrast-enhanced ultrasonography in patients with lymphedema.

Acronym

The study of contrast-enhanced ultrasonography in patients with lymphedema.

Scientific Title

The study of method to identify functional lymph vessels by contrast-enhanced ultrasonography in patients with lymphedema.

Scientific Title:Acronym

The study of contrast-enhanced ultrasonography in patients with lymphedema.

Region

Japan


Condition

Condition

lymphedema

Classification by specialty

Vascular surgery Plastic surgery

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

consider the efficacy of contrast-enhanced ultrasonography for the identification of functional lymphatic vessels

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Location,diameter and depth of lymphatic vessels, flow rate of lymph.

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Device,equipment

Interventions/Control_1

contrast-enhanced ultrasonography in 10 people of non-lymphedema.

Interventions/Control_2

contrast-enhanced ultrasonography in 50 patients of lymphedema.

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

Patient of lymphedema

Key exclusion criteria

Allergy for perflubutane and ICG.

Target sample size

60


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Maegawa Jiro

Organization

Yokohama city University

Division name

Plastic and Reconstructive Surgery

Zip code


Address

3-9 Fukuura,Kanazawa-ku, Yokohama 236-0004

TEL

045-787-2800

Email

maegawaj@med.yokohama-cu.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Maegawa Jiro

Organization

Yokohama city University

Division name

Plastic and Reconstructive Surgery

Zip code


Address

3-9 Fukuura,Kanazawa-ku, Yokohama 236-0004

TEL

045-787-2800

Homepage URL


Email

maegawaj@med.yokohama-cu.ac.jp


Sponsor or person

Institute

Yokohama city University

Institute

Department

Personal name



Funding Source

Organization

Yokohama city University

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


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

2013 Year 10 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

2013 Year 10 Month 01 Day

Date of IRB

2013 Year 09 Month 26 Day

Anticipated trial start date

2013 Year 10 Month 01 Day

Last follow-up date

2019 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

2013 Year 09 Month 26 Day

Last modified on

2020 Year 01 Month 21 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000013875


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name