UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000006720
Receipt number R000007943
Scientific Title Bone augmentation with tissue engineered bone
Date of disclosure of the study information 2011/11/14
Last modified on 2012/10/23 23:23:01

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Basic information

Public title

Bone augmentation with tissue engineered bone

Acronym

Bone augmentation with tissue engineered bone

Scientific Title

Bone augmentation with tissue engineered bone

Scientific Title:Acronym

Bone augmentation with tissue engineered bone

Region

Japan


Condition

Condition

Atrophy of alveolar bone

Classification by specialty

Oral surgery Dental medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Evaluation of bone regeneration using tissue engineered bone which composed of autogenous mesenchymal stem cells and scaffolds

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The evaluation of safety and clinical efficacy of tissue engineered 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

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Maneuver

Interventions/Control_1

Transplantation of tissue engineered bone

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

The patients who desire to undergo bone regeneration and agree with this treatment.

Key exclusion criteria

Patient who have severe complications, infectious disease, or other special conditions that is not appropriate to undergo this study.

Target sample size

100


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Minoru Ueda

Organization

Nagoya University Hospital

Division name

Oral and Maxillofacial Surgery

Zip code


Address

65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, 466-8550, Japan

TEL


Email



Public contact

Name of contact person

1st name
Middle name
Last name

Organization

Nagoya University Hospital

Division name

Oral and Maxillofacial Surgery

Zip code


Address

65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, 466-8550, Japan

TEL


Homepage URL


Email



Sponsor or person

Institute

Department of Oral and Maxillofacial Surgery, Nagoya University Hospital

Institute

Department

Personal name



Funding Source

Organization

The Ministry of Education,Culture,Sports,Science & Technology in Japan

Organization

Division

Category of Funding Organization

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

2011 Year 11 Month 14 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

2000 Year 09 Month 22 Day

Date of IRB


Anticipated trial start date

2001 Year 11 Month 01 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

2011 Year 11 Month 14 Day

Last modified on

2012 Year 10 Month 23 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000007943