UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000020480
Receipt number R000004356
Scientific Title REtrospective multicenter AnaLysis for FemoroPopliteal stent registry
Date of disclosure of the study information 2016/01/07
Last modified on 2016/01/21 18:50:17

* 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

REtrospective multicenter AnaLysis for FemoroPopliteal stent registry

Acronym

REAL FP

Scientific Title

REtrospective multicenter AnaLysis for FemoroPopliteal stent registry

Scientific Title:Acronym

REAL FP

Region

Japan


Condition

Condition

Peripheral artery disease

Classification by specialty

Cardiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the long term patency after nitinol stenting for femoro-popliteal lesion

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Primary patency

Key secondary outcomes



Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


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

symptoms due to the femoro-popliteal lesions (Rutherford 2-6) that affected the quality of life in spite of excises and medications.

Key exclusion criteria

We excluded those underwent angioplasty alone, those underwent stenting in the restenotic lesions and those presenting with acute or sub-acute limb ischemia with nitinol stents deployment. Patients whom we could not follow up at 6 month were also excluded from the analysis

Target sample size

742


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Osamu Iida

Organization

Kansai Rosai Hospital

Division name

Cardiovascular center

Zip code


Address

3-1-69, Inabaso, Amagasaki city, Hygo

TEL

06-6416-1221

Email

iida.osa@gmail.com


Public contact

Name of contact person

1st name
Middle name
Last name Osamu Iida

Organization

Kansai Rosai Hospital

Division name

Cardiovascular center

Zip code


Address

3-1-69, Inabaso, Amagasaki city, Hyogo

TEL

06-6416-1221

Homepage URL


Email

iida.osa@gmail.com


Sponsor or person

Institute

Kansai Rosai Hospital, cardiovascular center

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


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

2016 Year 01 Month 07 Day


Related information

URL releasing protocol


Publication of results

Published


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results

Long term results after endovascular therapy for patient presenting FP lesions were acceptable.

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

2004 Year 04 Month 01 Day

Date of IRB


Anticipated trial start date

2004 Year 04 Month 01 Day

Last follow-up date

2010 Year 05 Month 01 Day

Date of closure to data entry

2010 Year 05 Month 01 Day

Date trial data considered complete

2010 Year 05 Month 01 Day

Date analysis concluded



Other

Other related information

The rate of surgical conversion was low.


Management information

Registered date

2016 Year 01 Month 07 Day

Last modified on

2016 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=R000004356


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name