UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000007325
Receipt number R000008623
Scientific Title The Effect of Gingival Melanin Depigmentaion by Dental Lazer Treatment.
Date of disclosure of the study information 2012/02/18
Last modified on 2012/02/18 10:12:29

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

The Effect of Gingival Melanin Depigmentaion by Dental Lazer Treatment.

Acronym

The Effect of Gingival Melanin Depigmentaion by Dental Lazer Treatment.

Scientific Title

The Effect of Gingival Melanin Depigmentaion by Dental Lazer Treatment.

Scientific Title:Acronym

The Effect of Gingival Melanin Depigmentaion by Dental Lazer Treatment.

Region

Japan


Condition

Condition

Gingival Melanin Depigmentaion

Classification by specialty

Dental medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

There have been reported several methods to remove gingival hyperpigmentation, but, only a few reports are exist about comparing the effect of each method. Therefore, we will evaluate the effects both Er: YAG laser and CO2 laser treatment for gingival depigmentation numerically.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The hyperpigmentation area is put into 4 parts. Each part of the gingiva is treated as follows. Er:YAG laser: maxillary, left side, central incisor-cuspid, CO2 laser: mandibular, right side, central incisor-cuspid, abrasion surgery by carborundum points: maxillary, right side, central incisor-cuspid, and without treatment (as a control): mandibular, left side, central incisor-cuspid. The irradiation is carried out accoding to the manual for the hyperpigmentation. After treatment, the depigmentation effects will be evaluated by using Image J (ver1.43, NIH, Bethesda) about all methods.

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

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

The hyperpigmentation area is put into 4 parts. Each part of the gingiva is treated as follows. Er:YAG laser: maxillary, left side, central incisor-cuspid, CO2 laser: mandibular, right side, central incisor-cuspid, abrasion surgery by carborundum points: maxillary, right side, central incisor-cuspid, and without treatment (as a control): mandibular, left side, central incisor-cuspid. The irradiation is carried out accoding to the manual for the hyperpigmentation.

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


Not applicable

Gender

Male and Female

Key inclusion criteria

Smorker

Key exclusion criteria

Non-smokers

Target sample size

20


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Nobuo Yoshinari

Organization

Matsumoto dental university school of dentistry

Division name

department of periodontology

Zip code


Address

1780 gobara hirooka shiojiri nagano Japan

TEL


Email



Public contact

Name of contact person

1st name
Middle name
Last name Eisaku Nishida

Organization

Matsumoto dental university school of dentistry

Division name

department of periodontology

Zip code


Address

1780 gobara hirooka shiojiri nagano Japan

TEL


Homepage URL


Email



Sponsor or person

Institute

Matsumoto dental university

Institute

Department

Personal name



Funding Source

Organization

Matsumoto dental university

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

松本歯科大学病院(長野県)


Other administrative information

Date of disclosure of the study information

2012 Year 02 Month 18 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

2012 Year 02 Month 15 Day

Date of IRB


Anticipated trial start date

2012 Year 02 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

2012 Year 02 Month 18 Day

Last modified on

2012 Year 02 Month 18 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000008623


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name