UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000026265
Receipt number R000030161
Scientific Title Evaluation of bioabsorbable artifical bone for craniofacial surgery
Date of disclosure of the study information 2017/02/22
Last modified on 2018/02/24 21:36:50

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Basic information

Public title

Evaluation of bioabsorbable artifical bone for craniofacial surgery

Acronym

Efficiency of bioabsorbable artifical bone

Scientific Title

Evaluation of bioabsorbable artifical bone for craniofacial surgery

Scientific Title:Acronym

Efficiency of bioabsorbable artifical bone

Region

Japan


Condition

Condition

Craniofacial anomaly

Classification by specialty

Plastic surgery

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The efficicacy of artificial bone which is replaced to autologous bone is evaluated.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The bone volume of replacement to autologous bone

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

Historical

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

The bioresorbable artificial bone was put in the bone defect.

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

16 years-old >

Gender

Male and Female

Key inclusion criteria

The patients who had bone defects in the craniofacial region, and performed the operation for the defect.

Key exclusion criteria

The patients who could not come to the hospital over 1 years.

Target sample size

20


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Kazuo Kishi

Organization

Keio University School of Medicine

Division name

Department of Plastic and Reconstructive Surgery

Zip code


Address

35, Shinanomachi, Shinjuku-ku, Tokyo

TEL

+81353633814

Email

kkishi@a7.keio.jp


Public contact

Name of contact person

1st name
Middle name
Last name Yoshiaki Sakamoto

Organization

Keio University School of Medicine

Division name

Department of Plastic and Reconstructive Surgery

Zip code


Address

35, Shinanomachi, Shinjuku-ku, Tokyo

TEL

+81353633814

Homepage URL


Email

ysakamoto@z8.keio.jp


Sponsor or person

Institute

Keio University

Institute

Department

Personal name



Funding Source

Organization

None

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 02 Month 22 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

Main results already published

Date of protocol fixation

2015 Year 07 Month 24 Day

Date of IRB


Anticipated trial start date

2015 Year 07 Month 24 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 02 Month 22 Day

Last modified on

2018 Year 02 Month 24 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000030161


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name