UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000038946
Receipt number R000044402
Scientific Title Efficacy and safety of hair loss suppression by additional scalp cooling during breast cancer chemotherapy
Date of disclosure of the study information 2019/12/23
Last modified on 2022/07/11 19:53:07

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Basic information

Public title

Efficacy and safety of hair loss suppression by additional
scalp cooling during breast cancer chemotherapy

Acronym

scalp cooling

Scientific Title

Efficacy and safety of hair loss suppression by additional
scalp cooling during breast cancer chemotherapy

Scientific Title:Acronym

scalp cooling

Region

Japan


Condition

Condition

breast cancer

Classification by specialty

Breast surgery

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

For patients with a confirmed diagnosis of breast cancer who have undergone pre- and post-operative chemotherapy for stage I / II / III initial breast cancer, epilation by scalp cooling for epilation with frequent side effects Investigate whether there is an inhibitory effect and consider safety.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Evaluation of hair loss at the end of chemotherapy and during chemotherapy (CTCAE ver.4.0)
Hair loss of eyebrows and eyelashes
Whether wearing a hat or wig

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

Self control

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

[Device used] PAXMAN scalp cooling device (Century Medical Co., Ltd.)
[Cooling time] About 3 and a half hours
[Intervention period] Anthracycline 4 courses and taxane 4 courses are being administered, assuming intervention for patients with primary breast cancer.
[Administration drug] Both anthracycline (FEC, AC, EC) and taxane (DTX, PTX) are administered. Weight loss can be up to 25%. Anti-HER2 drugs may be included.

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

60 years-old >=

Gender

Female

Key inclusion criteria

1) Patients histologically diagnosed with breast cancer
2) Women who are over 20 years old and under 60 years old
3) Patients who are scheduled to undergo chemotherapy and hair loss is predicted
4) Patients who have given their consent in writing
5) Patients who are scheduled to have 8 or more courses of chemotherapy including anthracycline and taxane anticancer drugs before or after surgery (weight loss is up to 25%)

Key exclusion criteria

1) Patients with malignant blood disease
2) Patients with cold allergies
3) Patients with cold agglutinin disease
4) Patients with a tumor on the scalp
5) Patients receiving high-dose anticancer drugs as pretreatment for stem cell transplantation
6) Patients undergoing head radiation therapy

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Nana
Middle name
Last name Komatsu

Organization

Showa University

Division name

Breast center

Zip code

1428555

Address

1-5-8 Hatanodai Shinagawa Tokyo

TEL

0337848000

Email

nanakomatsu.0503@gmail.com


Public contact

Name of contact person

1st name Nana
Middle name
Last name Komatsu

Organization

Showa University

Division name

Breast center

Zip code

1428555

Address

1-5-8 Hatanodai Shinagawa Tokyo

TEL

0337848000

Homepage URL


Email

nana.k@med.showa-u.ac.jp


Sponsor or person

Institute

Showa University

Institute

Department

Personal name



Funding Source

Organization

Century Medical

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Showa University

Address

1-5-8 Hatanodai Shinagawa Tokyo

Tel

0337848000

Email

nanakomatsu.0503@gmail.com


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

2019 Year 12 Month 23 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

Completed

Date of protocol fixation

2019 Year 02 Month 14 Day

Date of IRB

2019 Year 04 Month 12 Day

Anticipated trial start date

2020 Year 01 Month 06 Day

Last follow-up date

2020 Year 09 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2019 Year 12 Month 20 Day

Last modified on

2022 Year 07 Month 11 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000044402


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name