None
Conditions
Interventions
Control group:Use of the Bai Tian E Intense Pulsed Light (IPL) Hair Removal Device
Experimental group:Use of the Bai Tian E Intense Pulsed Light (IPL) Hair Removal Device combined with light-conducting gel
Sponsors
Dematology Hospital of Southern Medical University
Eligibility
Sex/Gender
Female
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1.Aged 18–60 years, Asian (Chinese), healthy females; 2.Self-perceived sensitive skin; 3.Self-perceived excessive axillary hair and with hair removal demands; 4.History of using home-use hair removal devices; 5.Able to understand the trial procedures, voluntarily participate in the trial and sign a written informed consent form;
Exclusion criteria
Exclusion criteria: 1.Those who have applied any topical medications to the test sites within the past two months; 2.Those who have taken antihistamines within the past week or immunosuppressants within the past month; 3.Those with unresolved inflammatory dermatoses; 4.Patients with insulin-dependent diabetes mellitus; 5.Patients with asthma or other chronic respiratory diseases currently under treatment; 6.Those who have received anticancer chemotherapy within the past six months; 7.Patients with immunodeficiency or autoimmune diseases; 8.Women who are planning pregnancy, pregnant or lactating; 9.Those with obvious scars, pigmentation, atrophy, port-wine stains, sunburn, wounds, abrasions, tattoos or other skin defects on or near the skin test sites that may interfere with the evaluation of trial results; 10.Those who have received photorejuvenation, laser therapy or other facial cosmetic procedures that may affect skin condition within the past three months; 11.Those who have participated in similar facial trials, oral drug trials or other clinical trials within the past two months; 12.Subjects with highly sensitive constitutions, or known to be allergic to ingredients in cosmetics, daily chemicals, alcohol, rubber or medications; 13.Those who need to be chronically exposed to outdoor sunlight due to work or other reasons; 14.Those with other iatrogenic conditions that may affect the trial results (e.g., history of coagulation disorders, severe hyperglycemia, hypertension, hyperlipidemia, mental illness or other major diseases); 15.Those deemed unsuitable for trial participation by clinical assessment; 16.Those who are non-voluntary participants or unable to complete the required trial procedures as instructed;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hair count; | — |
Secondary
| Measure | Time frame |
|---|---|
| Skin a* value;Hair density;Stratum corneum moisture content;NRS score;Skin ITA° value;Skin firmness;Transepidermal water loss;Skin elasticity; | — |
Countries
China
Contacts
Public ContactYe Li
Dematology Hospital of Southern Medical University
Outcome results
None listed