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Clinical efficacy of fire needle combined with Xiaoban tincture in the treatment of localized alopecia areata

Clinical efficacy of fire needle combined with Xiaoban tincture in the treatment of localized alopecia areata

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070697
Enrollment
Unknown
Registered
2023-04-20
Start date
2023-04-19
Completion date
Unknown
Last updated
2023-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

alopecia areata

Interventions

Fire needle + Xiaoban tincture group (left quadrant of group 1):One hour before each acupuncture treatment, compound lidocaine cream will be applied to the selected alopecia area and treated with fire
Xiaoban tincture group (right quadrant of group 1):The operator will apply Xiaoban tincture to the local head affected area, 1mL each time (about 7 sprays), and start to smear from the center of the a
Fire needle group (left quadrant of group 2):One hour before each acupuncture treatment, compound lidocaine cream will be applied to the selected alopecia area and treated with fire needle.
Negative control group (right quadrant of group 2):The right quadrant of group 2 served as negative control without treatment.

Sponsors

The First Affiliated Hospital of Guangzhou University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Patients who were primary cases in skin clinic without any treatment; (2) Age >= 18 years old, regardless of sex; (3) Patients who met the diagnostic criteria of localized alopecia areata: the number of alopecia plaques >= 2, plaque diameter >= 1.5cm, alopecia area < 50%; (4) Patients who voluntarily participated in this study, signed a written informed consent form, and were willing to cooperate with the follow-up.

Exclusion criteria

Exclusion criteria: (1) Patients with Alopecia Areata (AA) except localized type; (2) Patients with other forms of patchy alopecia (such as trichomadesis, traction alopecia, syphilitic alopecia); (3) Patients with obvious spontaneous regeneration of peripheral hair; (4) Patients who received intrafocal or systemic corticosteroids or any alopecia areata treatment 2 months before the study; (5) Patients with another skin disease affecting the scalp, such as eczema; (6) Patients with diabetes or severe liver and kidney disease; (7) Patients with hemorrhage; (8) Patients who have a history of immunodeficiency diseases (such as HIV, etc.), or a history of cancer, malignant tumors, or autoimmune diseases, or severe cardiovascular or cerebrovascular diseases, or other diseases that may significantly reduce life expectancy; (IX) Patients who have any history of diseases that may affect programme compliance (such as severe mental disorders, cognitive impairment, substance abuse or addiction, etc.); (10) Pregnant or lactating women, or fertile women who are unwilling / unable to use effective contraceptive measures; (11) Patients who known to be allergic to Xiaoban tincture, lidocaine cream, iodophor or 75% alcohol in this study; (12)Patients who have participated in any drug clinical trial in the 6 months prior to the screening test; (13) Patients with dizzy needles.

Design outcomes

Primary

MeasureTime frame
Effective rate of clinical efficacy;

Secondary

MeasureTime frame
The number of malnourished hair in alopecia area under dermatoscope;Dermatology Life Quality Index(DLQI);Visual Analogue Scale;Initial reaction time of hair regeneration;Patient satisfaction;Percentage of hair regeneration;

Countries

China

Contacts

Public ContactLiu Jing

The First Affiliated Hospital of Guangzhou University of Chinese Medicine

lj135088@163.com+86 13556162738

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026