Department of Clinical Oncology, Prince of Wales Hospital
Hong Kong, 852
NCT Number: NCT04630080
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.
This study is active but is not currently recruiting participants.
Notify Me18 year–70 year
Female
Interventional
Not applicable
Hong Kong, 852
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,
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
Scalp cooling is a physical method to reduce chemotherapy-induced alopecia
Time frame: 2 year
Time frame: 2 years
It will be assessed by study tool ALOPECIA ASSESSMENT BY PATIENT AND WIG USE FORM
Time frame: 2 years
It will be assessed by study tool EORTC QLQ-30
Time frame: 2 years
It will be assessed by study tool EORTC QLQ - BR23
Time frame: 2 years
It will be assessed by COMFORT SCALE FORM.
Chinese University of Hong Kong
Other
Scalp Cooling Study for the Prevention of Chemotherapy-induced Alopecia in Chinese Breast Cancer Patients
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