UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000030887
Receipt number R000035267
Scientific Title Clinical study of endovascular laser ablation for varicose vein
Date of disclosure of the study information 2018/01/26
Last modified on 2019/03/04 12:11:53

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Basic information

Public title

Clinical study of endovascular laser ablation for varicose vein

Acronym

Clinical study of endovascular laser ablation for varicose vein

Scientific Title

Clinical study of endovascular laser ablation for varicose vein

Scientific Title:Acronym

Clinical study of endovascular laser ablation for varicose vein

Region

Japan


Condition

Condition

varicose veins

Classification by specialty

Vascular surgery

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Study the safety and effectiveness of newly developed endovascular laser equipment and fiber
for varicose vein

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Venous occlusion rate at 12 weeks after surgery

Key secondary outcomes

The incidence of adverse events on 1 day, 1 week, 4 weeks and 12 weeks after surgery


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

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

Endovascular laser ablation for varicose vein

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

100 years-old >=

Gender

Male and Female

Key inclusion criteria

Patients satisfying all the indications for endovascular therapy in "Endovascular treatment guidelines for varicose veins"

Patients who agreed to participate in this study

Patients who can go to the outpatient hospital until 12 weeks after surgery

Key exclusion criteria

Patients falling under any of the exclusion criteria in "Endovascular treatment guidelines for varicose veins"

Patient judged inappropriate by the attending physician

Target sample size

10


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Taijiro Sueda

Organization

Hiroshima University Hospital

Division name

Cardiovascular Surgery

Zip code


Address

1-2- 3 Kasumi Minami-ku Hiroshima-city

TEL

082-257-5215

Email

sueda@hiroshima-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Tatsuya Kurosaki

Organization

Hiroshima University Hospital

Division name

Cardiovascular Surgery

Zip code


Address

1-2- 3 Kasumi Minami-ku Hiroshima-city

TEL

082-257-5215

Homepage URL


Email

kurosakt@hiroshima-u.ac.jp


Sponsor or person

Institute

Hiroshima University

Institute

Department

Personal name



Funding Source

Organization

Japan Agency for Medical Research and Development

Organization

Division

Category of Funding Organization

Japanese Governmental office

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

2018 Year 01 Month 26 Day


Related information

URL releasing protocol


Publication of results

Partially published


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

2018 Year 01 Month 15 Day

Date of IRB


Anticipated trial start date

2018 Year 02 Month 01 Day

Last follow-up date

2019 Year 02 Month 28 Day

Date of closure to data entry

2019 Year 02 Month 28 Day

Date trial data considered complete

2019 Year 02 Month 28 Day

Date analysis concluded

2019 Year 03 Month 31 Day


Other

Other related information



Management information

Registered date

2018 Year 01 Month 19 Day

Last modified on

2019 Year 03 Month 04 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000035267


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name