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NCT Number: NCT04630080

Alopecia Prevention Scalp Cooling in Chinese Breast Cancer Patients

The Orbis Paxman Hair Loss Prevention System is a new equipment introduced to Hong Kong in 2017. Although this device has been widely used in the United States, Europe and Australia, acceptability, efficacy and safety data in Chinese have not yet been available. The objective of this prospective study is to collect clinical data in Chinese patients using the Orbis Paxman Hair Loss Prevention System to prevent chemotherapy-induced alopecia.

This project seeks to demonstrate that the Orbis Paxman Hair Loss Prevention System is safe and effective in reducing chemotherapy-induced alopecia in woman with breast cancer undergoing neoadjuvant or adjuvant chemotherapy.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

18 year–70 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Department of Clinical Oncology, Prince of Wales Hospital

Hong Kong, 852

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

i) New diagnosis of breast cancer stage I-III

ii) Chinese ethnicity

iii) ECOG 0-1

iii) Planning to undergo neoadjuvant or adjuvant chemotherapy with curative intent

iv) Chemotherapy must be planned for at least 4 cycles of full-dose anthracycline and/or taxane based chemotherapy regimen,

  • Defined as one of the following regimens:
  • Adriamycin 60 mg/m2 with cyclophosphamide 600 mg/m2 for 4 cycles (AC) > 5-Fluorouracil 500 mg/m2, Epirubicin 100mg/m2, and cyclophosphamide 500 mg/m2 for 3 cycles, followed by Docetaxel 100 mg/m2 for 3 cycles (FEC-D)
  • AC x 4 cycles, followed by Docetaxel 100 mg/m2 for 4 cycles (AC-D)
  • AC x 4 cycles, followed by Paclitaxel 175 mg/m2 for 4 cycles (AC-P)
  • Docetaxel 75 mg/m2 with cyclophosphamide 600 mg/m2 for 4-6 cycles (DC)
  • Docetaxel 75 mg/m2 with carboplatin AUC of 5-6 for 4-6 cycles (DCb)
  • Concurrent trastuzumab and/or pertuzumab at standard doses is allowed.
  • Administration of chemotherapy on a dose dense schedule with GCSF is allowed.

v) Adequate organ functions vi) Normal thyroid stimulating hormone vii) Subjects with history of diabetes must have acceptable HBA1c on study entry viii) Subjects who provide consent and are mentally competent and able to fill in study questionnaires

Exclusion criteria

i) Subjects with any other concurrent malignancy including hematological malignancies (i.e. leukemia or lymphoma)

ii) Subjects with cold agglutinin disease or cold urticaria

iii) Age ≥ 70 years

iv) Personal history of migraines, cluster or tension headaches as defined as actual medical diagnosis by a physician and/ or prescribed medications. If personal history of migraines was related to a past medical problem that is now resolved, subject may go on study at the discretion of the Principal Investigator.

v) Elevated liver enzymes or bilirubin defined as 3 times the upper limits of normal

vi) Serum Albumin < 3.0

vii) Subjects with anemia (defined as a hemoglobin < 10)

viii) Subjects who have lichen planus or lupus, or other dermatological conditions involving scalp

ix) Subjects who are underweight (defined as a BMI < 18.5)

x) Subjects who have had previous chemotherapy exposure

Treatment and study plan

scalp cooling

Device

Scalp cooling is a physical method to reduce chemotherapy-induced alopecia

Primary outcomes

  1. The success rate of scalp cooling in preventing chemotherapy-induced alopecia

    Time frame: 2 year

Secondary outcomes

  1. The rate of preceived hair preservation during and after completion of chemotherapy

    Time frame: 2 years

    It will be assessed by study tool ALOPECIA ASSESSMENT BY PATIENT AND WIG USE FORM

  2. The quality of life during and after completion of chemotherapy

    Time frame: 2 years

    It will be assessed by study tool EORTC QLQ-30

  3. The disease site specific quality of life during and after completion of chemotherapy

    Time frame: 2 years

    It will be assessed by study tool EORTC QLQ - BR23

  4. The incidence of treatment-emergent adverse events of scalp cooling

    Time frame: 2 years

    It will be assessed by COMFORT SCALE FORM.

Sponsors and collaborators

Lead sponsor

Chinese University of Hong Kong

Other

Registry information

Official study title

Scalp Cooling Study for the Prevention of Chemotherapy-induced Alopecia in Chinese Breast Cancer Patients

Important dates

Study start
2021
Primary completion
2026
Study completion
2027
First posted
Nov 16, 2020
Registry last updated
Jan 9, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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