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A Clinical Study on the Treatment of Scalp Seborrheic Dermatitis with Scalp Complex Acids

A Clinical Study on the Treatment of Scalp Seborrheic Dermatitis with Scalp Complex Acids

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097253
Enrollment
Unknown
Registered
2025-02-15
Start date
2024-02-12
Completion date
Unknown
Last updated
2025-02-24

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

Conditions

Seborrheic Dermatitis

Interventions

Scalp Oil-Control and Balancing Complex Acids Group:The subjects in this group used Ximeien scalp oil control balance compound acid once a week for a total of 4 times.
Selenium Sulfide Lotion:Topical application of selenium sulfide lotion, twice a week for a total of eight applications.
Complete Scalp Care Products Group:Topical application of Oil-Control Balancing Complex Acids (once a week, total of 4 applications), along with Oil-Control Anti-Dandruff Shampoo (twice a week, total

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Patients diagnosed with scalp seborrheic dermatitis based on the diagnostic criteria outlined in the Chinese Dermatology and Venereology (Clinical Edition). 2.Aged 18 to 60 years, regardless of gender. 3.Clinical manifestations of scalp seborrheic dermatitis, including erythema, papules, scales, pruritus, and greasiness on the scalp. 4.Dermoscopic evidence of scalp seborrheic dermatitis, such as inflammatory papules, erythema, vascular dilation, and scaling. 5.Patients who are willing to participate in the study and have signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Patients who have a history of treatment of scalp seborrheic dermatitis, including oral or topical medications, other acid-based products, or functional scalp care products within the past two weeks. 2.Patients who have a history of allergy to any ingredient in the products used in this study. 3.Refusal to accept or rejection of the study protocol. 4.Presence of hyperthyroidism, hypothyroidism, severe malnutrition, endocrine disorders, autoimmune diseases, or other major diseases involving organs such as the heart, liver, lungs, or brain. 5.Patients who have a history of psychiatric disorders or mental illness. 6.Pregnant or breastfeeding women.

Design outcomes

Primary

MeasureTime frame
Erythema Severity Score;Papule Severity Score;

Secondary

MeasureTime frame
Observation, Recording, and Management of Adverse Events;

Countries

China

Contacts

Public ContactMao Lin

West China Hospital, Sichuan University

linmao@wchscu.cn+86 133 3027 0780

Outcome results

None listed

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