UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000019077
Receipt number R000022057
Scientific Title Safety of Percutaneous Cryoablation in Patients with Painful Bone and Soft Tissue Tumors: A Single Center Prospective Study (SCIRO-1502)
Date of disclosure of the study information 2015/12/01
Last modified on 2020/09/14 10:38:17

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Basic information

Public title

Safety of Percutaneous Cryoablation in Patients with Painful Bone and Soft Tissue Tumors: A Single Center Prospective Study (SCIRO-1502)

Acronym

Cryoablation for painful bone and soft tissue tumors (SCIRO-1502)

Scientific Title

Safety of Percutaneous Cryoablation in Patients with Painful Bone and Soft Tissue Tumors: A Single Center Prospective Study (SCIRO-1502)

Scientific Title:Acronym

Cryoablation for painful bone and soft tissue tumors (SCIRO-1502)

Region

Japan


Condition

Condition

Painful bone and soft tissue tumor

Classification by specialty

Orthopedics Radiology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the safety of percutaneous cryoablation for painful bone and soft tissue tumors.

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Phase I


Assessment

Primary outcomes

Number of adverse events (Time Frame: 1 month post-cryoablation)

Key secondary outcomes

Difference in VAS, efficacy, and imagings 1 month after cryoablation


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 Maneuver

Interventions/Control_1

Following percutaneously inserting electrode(IceSeed or IceRod; Galil Medical, Yokneam, Israel), cryoablation for painful bone and soft tissue tumor is performed using CryoHit (Galil Medical); cryoablation is performed in two cycles of maximum 15 minutes freezing and at least 2 minutes thawing.

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

1) Painful bone and soft tissue tumor with resistance of medication.
2) Pathologically confirmed painful bone and soft tissue tumor.
3) Target lesion is evaluated with imagings.
4) Life expectancy >= 1 month.
5) Written informed consent.
6) Patient's age is more than 20 years old.
7) Not a candidate for surgery or refuse surgery.

Key exclusion criteria

1) Vital organ and/or vessel on the needle route.
2) Patient has the following comorbidities.
a) Heart failure (NYHA >= III)
b) Active infection except for virus hepatitis
3) Body temperature of 38 degree or more.
4) Target lesion is not able to be evaluated with imagings.
5) Pregnant.
6) Worse bone fracture caused by cryoablation.
7) Worse quality of life caused by cryoablation.
8) Inadequate cardiac, hepatic, renal, respiratory, coagulation, and bone marrow functions.
9) Not eligible determined by the responding physician.

Target sample size

10


Research contact person

Name of lead principal investigator

1st name Toshihiro
Middle name
Last name Iguchi

Organization

Okayama University Hospital

Division name

Department of Radiology

Zip code

7008558

Address

2-5-1 Shikata-cho, Kita-ku, Okayama city

TEL

+81-86-235-7315

Email

susumu@cc.okayama-u.ac.jp


Public contact

Name of contact person

1st name Toshihiro
Middle name
Last name Iguchi

Organization

Okayama University Hospital

Division name

Department of Radiology

Zip code

7008558

Address

2-5-1 Shikata-cho, Kita-ku, Okayama city

TEL

+81-86-235-7313

Homepage URL


Email

iguchi@cc.okayama-u.ac.jp


Sponsor or person

Institute

Okayama University Hospital

Institute

Department

Personal name



Funding Source

Organization

JAPAN SOCIETY FOR THE PROMOTION OF SCIENCE

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

Dept. of Radiology, Okayama University Medical School

Address

2-5-1 Shikata-cho, Kita-ku, Okayama city

Tel

+81-86-235-6503

Email

radiol@cc.okayama-u.ac.jp


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

2015 Year 12 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

Terminated

Date of protocol fixation

2015 Year 09 Month 19 Day

Date of IRB

2015 Year 09 Month 26 Day

Anticipated trial start date

2015 Year 12 Month 01 Day

Last follow-up date

2018 Year 12 Month 14 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2015 Year 09 Month 19 Day

Last modified on

2020 Year 09 Month 14 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000022057


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name