UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000016044
Receipt number R000018648
Scientific Title Image guided cryoablation for malignant bone and soft tissue tumor
Date of disclosure of the study information 2014/12/26
Last modified on 2014/12/24 13:50:59

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Basic information

Public title

Image guided cryoablation for malignant bone and soft tissue tumor

Acronym

Cryoablation for malignant bone and soft tissue tumor

Scientific Title

Image guided cryoablation for malignant bone and soft tissue tumor

Scientific Title:Acronym

Cryoablation for malignant bone and soft tissue tumor

Region

Japan


Condition

Condition

Recurrent or metastatic bone and soft tissue tumors

Classification by specialty

Orthopedics Radiology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To analyze the clinical outcome of image guided cryoablation for malignant bone and soft tissue tumors to elucidate the problems surrounding this procedure.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase

Phase II


Assessment

Primary outcomes

Effectiveness against the tumor will be analyzed at 1 month after treatment and every 3 month afterward using Xp, CT, and MRI. Pain will be assessed prior to the treatment, 1 day and 1 week after the treatment, and every 3 month afterward using the VAS.

Key secondary outcomes



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

Maneuver

Interventions/Control_1

Recurrent or metastatic bone and soft tissue tumor

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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Recurrent or metastatic bone and soft tissue tumor

Key exclusion criteria

1. Cases with coagulation disorder or hemorrhagic tendency.
2. Lesions that are adjacent to vital organs.
3. Cases with systemic or local infection near the treatment site.

Target sample size

30


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Hideo Morioka

Organization

Keio University School of Medicine

Division name

Department of orthopaedic surgery

Zip code


Address

35 Shinanomachi, Shinjuku-ku, Tokyo

TEL

03-5363-3812

Email

morioka@z3.keio.jp


Public contact

Name of contact person

1st name
Middle name
Last name Hideo Morioka

Organization

Keio University School of Medicine

Division name

Department of orthopaedic surgery

Zip code


Address

35 Shinanomachi, Shinjuku-ku, Tokyo

TEL

03-5363-3812

Homepage URL


Email

morioka@z3.keio.jp


Sponsor or person

Institute

Keio University School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Non applicable

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

2014 Year 12 Month 26 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

Open public recruiting

Date of protocol fixation

2011 Year 08 Month 23 Day

Date of IRB


Anticipated trial start date

2011 Year 08 Month 23 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

2014 Year 12 Month 24 Day

Last modified on

2014 Year 12 Month 24 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000018648


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name