UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000004986
Receipt number R000005929
Scientific Title The prospective study about the color change and reproducibility in the nipple areola tattoo
Date of disclosure of the study information 2011/02/01
Last modified on 2023/08/11 12:29:06

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Basic information

Public title

The prospective study about the color change and reproducibility in the nipple areola tattoo

Acronym

The prospective study about the color change and reproducibility in the nipple areola tattoo

Scientific Title

The prospective study about the color change and reproducibility in the nipple areola tattoo

Scientific Title:Acronym

The prospective study about the color change and reproducibility in the nipple areola tattoo

Region

Japan


Condition

Condition

nipple areola color asymmetry

Classification by specialty

Plastic surgery

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the color change, the color reproducibility, and the difference by the skin thickness in a medical tattoo.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Based on a clinical photograph (pre-ope, post 1 week, post 1 month, post 3 months, post 6 months, post 1 year), we evaluate the difference with the color chart, the difference with the normal side, the serial change of color using an index (a histogram mean) of the brightness.

Key secondary outcomes

Furthermore, We evaluate the color difference due to the type of the breast reconstruction.


Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


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

Female

Key inclusion criteria

The women (20 years or older) who can judge to participate in a study by own intention.

Key exclusion criteria

When subjects choose not to participate in a study, or withdraw the declaration of participating intention.

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Hiroki
Middle name
Last name Mori

Organization

Tokyo Medical and Dental University

Division name

Plastic and Reconstructive surgery

Zip code

113-8510

Address

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

TEL

81-3-5803-5923

Email

moriplas@tmd.ac.jp


Public contact

Name of contact person

1st name Hiroki
Middle name
Last name Mori

Organization

Tokyo Medical and Dental University

Division name

Plastic and Reconstructive surgery

Zip code

113-8510

Address

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

TEL

81-3-5803-5923

Homepage URL


Email

moriplas@tmd.ac.jp


Sponsor or person

Institute

Plastic and Reconstructive surgery, Tokyo Medical and Dental University

Institute

Department

Personal name



Funding Source

Organization

none

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

Tokyo Medical and Dental univ

Address

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

Tel

03-3813-6111

Email

tiken.crc@tmd.ac.jp


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 02 Month 01 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

60

Results


Results date posted


Results Delayed

Delay expected

Results Delay Reason

under submission

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

No longer recruiting

Date of protocol fixation

2010 Year 04 Month 27 Day

Date of IRB

2010 Year 04 Month 27 Day

Anticipated trial start date

2010 Year 05 Month 01 Day

Last follow-up date

2015 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded

2019 Year 12 Month 31 Day


Other

Other related information

prospective study
now going on.


Management information

Registered date

2011 Year 01 Month 31 Day

Last modified on

2023 Year 08 Month 11 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000005929


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name