UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000030157
Receipt number R000034433
Scientific Title Development of a self-care program for thepatients undergoing lymphaticovenular anastomosis
Date of disclosure of the study information 2017/12/10
Last modified on 2017/11/28 17:32:10

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Basic information

Public title

Development of a self-care program for thepatients undergoing lymphaticovenular anastomosis

Acronym

Development of a self-care program for thepatients undergoing LVA

Scientific Title

Development of a self-care program for thepatients undergoing lymphaticovenular anastomosis

Scientific Title:Acronym

Development of a self-care program for thepatients undergoing LVA

Region

Japan


Condition

Condition

secondary lymphedema

Classification by specialty

Breast surgery Plastic surgery Rehabilitation medicine
Nursing

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To clarify the effect of preoperative complex decongestive therapy(CDT) on treatment results of LVA

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

A value of segmental body composition measurement

Key secondary outcomes

Limb circumference length
Limb volume
Viscoelasticity on skin surface
MR image
Ultrasonic echo image of the subcutaneous tissue
Lymphedema related symptoms


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Dose comparison

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Behavior,custom

Interventions/Control_1

group of high implementation rate of preoperative CDT

Interventions/Control_2

group of low implementation rate of preoperative CDT

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

100 years-old >

Gender

Female

Key inclusion criteria

1)unilateral secondary lymphedema
2)>=6 month from radiation treatment and /or chemotherapy
3)got the medical doctore's approval to take CDT, LVA and some medical devices n this study(e.g. MRI)
4)already applied with compression garment

Key exclusion criteria

1)Cancer recurrence
2)<6 month from hospital CDT

Target sample size

40


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Chika Oshima

Organization

Nagoya University,
Graduate School of Medicine

Division name

Department of Nursing

Zip code


Address

1-1-20 Daiko-minami Higashi-ku Nagoya city, Aichi 461-8673 Japan

TEL

052-719-3101

Email

chika@met.nagoya-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Chika Oshima

Organization

Nagoya University, Graduate School of Medicine

Division name

Department of Nursing

Zip code


Address

1-1-20 Daiko-minami Higashi-ku Nagoya city, Aichi 461-8673 Japan

TEL

052-719-3101

Homepage URL


Email

chika@met.nagoya-u.ac.jp


Sponsor or person

Institute

Nagoya University, Graduate School of Medicine, Department of Nursing

Institute

Department

Personal name



Funding Source

Organization

Japan Society for the Promotion of Science

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

2017 Year 12 Month 10 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 12 Month 22 Day

Date of IRB


Anticipated trial start date

2018 Year 01 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 11 Month 28 Day

Last modified on

2017 Year 11 Month 28 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000034433


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name