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A clinical study protocol to evaluate the efficacy and safety of supramolecular salicylic acid in the treatment of rosacea

Evaluation of efficacy and safety of supramolecular salicylic acid in the treatment of rosacea

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200065218
Enrollment
Unknown
Registered
2022-11-01
Start date
2020-03-19
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Rosacea

Interventions

Control group:placebo (30% supramolecular salicylic acid mimic)

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1) Patients with papulopustular rosacea as a major phenotype according to Standard classification and pathophysiology of rosacea: The 2017 update by the National Rosacea Society Expert Committee (Annex 1); 2) Patients aged between 18-60 years; 3) Patients must agree to participate in the current protocol and sign a written informed consent.

Exclusion criteria

Exclusion criteria: 1) Patients with other facial skin diseases such melisma, freckles and asseborrheic dermatitis, which may affect the determination of the study results; 2) Patients who are allergic to any ingredients of the study drugs or patients with an allergic constitution; 3) Females who are pregnant, planning a pregnancy, or breastfeeding; 4) Patients with acne; 5) Patients taking oral antibiotics (such as minocycline, doxycycline), adrenergic receptor blockers (such as carvedilol) and other drugs for treating rosacea (such as hydroxychloroquine, etc.) during the prior 4 weekspatients taking topical Fusidic acid cream, azelaic acid, brimonidine and other drugs for treating rosacea; patients who had received physical therapy to treat rosacea; patients who had received salicylic acid and alpha-hydroxy acid treatment; 6) Patients taking oral retinoids during the prior 2 months (or oral acitrefin during the prior 6 months); 7) Patients taking topical tacrolimus during the prior 3 months 8) Patients who received facial injection or surgery during the prior 2 months; 9) Patients with immunodeficiency diseases.

Design outcomes

Primary

MeasureTime frame
Lesion reduction rate;Total effective rate;

Secondary

MeasureTime frame
Investigator’s Global Assessment (IGA);Investigator Severity Assessement (ISA);VISIA red area value improvement rate;

Countries

China

Contacts

Public ContactXian Jiang
jennyxianj@163.com+86 028 85423319

Outcome results

None listed

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