UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000022347
Receipt number R000025760
Scientific Title The evaluation of clinical outcomes and patient-reported outcomes following treatment of intrabony defects using a natural bone mineral and GTR
Date of disclosure of the study information 2016/05/30
Last modified on 2017/12/07 12:09:23

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Basic information

Public title

The evaluation of clinical outcomes and patient-reported outcomes following treatment of intrabony defects using a natural bone mineral and GTR

Acronym

The evaluation of intrabony defects treatment using a natural bone mineral and GTR

Scientific Title

The evaluation of clinical outcomes and patient-reported outcomes following treatment of intrabony defects using a natural bone mineral and GTR

Scientific Title:Acronym

The evaluation of intrabony defects treatment using a natural bone mineral and GTR

Region

Japan


Condition

Condition

periodontitis

Classification by specialty

Dental medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

This study evaluates the clinical outcomes and patient-reported outcomes following treatment of intrabony defects with application of a natural bone mineral (Bio-Oss) and guided tissue regeneration (Bio-Gide) compared with autograft and Bio-Gide. Using Bio-Oss has the advantage in both patient-related outcome and operation time, since the clinical outcome is comparable to using autograft.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

clinical attachment level(6 month 12 month)

Key secondary outcomes

patient-related outcome


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -but assessor(s) are blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

A natural bone mineral (Bio-Oss) and guided tissue regeneration (Bio-Gide)

Interventions/Control_2

Autograft and guided tissue regeneration (Bio-Gide)

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

80 years-old >

Gender

Male and Female

Key inclusion criteria

intrabony defect
PPD: Probing pocket depth over 6mm.
Radiographic evidence of an intrabony component over 4mm.

Key exclusion criteria

(1) Systemic disease that could influence the outcome of therapy.
(2) Systemic antibiotics had been used within at least 3 months.
(3) Smokers.

Target sample size

40


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Izumi Yuichi

Organization

Tokyo Medical and Dental University

Division name

Department of Periodontology

Zip code


Address

1-5-45 Yushima, Bunkyo-ku, Tokyo

TEL

03-5803-5488

Email

y-izumi.peri@tmd.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Hoshi Shu

Organization

Tokyo Medical and Dental University

Division name

Department of Periodontology

Zip code


Address

1-5-45 Yushima, Bunkyo-ku, Tokyo

TEL

03-5803-5488

Homepage URL


Email

hosperi@tmd.ac.jp


Sponsor or person

Institute

Tokyo Medical and Dental University

Institute

Department

Personal name



Funding Source

Organization

self funding

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 05 Month 30 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

2016 Year 05 Month 30 Day

Date of IRB


Anticipated trial start date

2016 Year 09 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

2016 Year 05 Month 18 Day

Last modified on

2017 Year 12 Month 07 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000025760


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name