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Efficacy of a Linoleic Acid-Ceramide Containing Moisturizer as an adjunctive andpreventive therapy in the treatment of mild to moderate psoriasis vulgaris

Efficacy of a Linoleic Acid-Ceramide Containing Moisturizer as an adjunctive andpreventive therapy in the treatment of mild to moderate psoriasis vulgaris:A Multicenter Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-15007138
Enrollment
Unknown
Registered
2015-08-31
Start date
2013-01-10
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

psoriasis vulgaris

Interventions

Control Group (C1):mometasone furoate 0.1% cream once daily
Treatment Group (T1):mometasone furoate 0.1% cream +moisturizer
Control Group (C2):mometasone furoate 0.1% cream prn
Treatment Group (T2):mometasone furoate 0.1% cream prn+ moisturizer once daily

Sponsors

Rui Jin Hospital, Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Clinically Diagnosed psoriasis vulgaris patients; 2. BSA less than 10%, PASI score <=10; 3. No age or gender limitation; 4. Participant or legal guardian fully understands the content of the clinical trial, is willing to attend the research voluntary andsign the informed consent form; 5. Physical examination is qualified, participant does not have previous severe systemic disease.

Exclusion criteria

Exclusion criteria: 1. physical examination failed to qualify for enrollment; 2. during gestational andlactation period; 3. known allergic history toward drug or moisturizer under study; 4. severe psoriasis vulgaris patients; 5. involved in any other clinical trial three months before enrollment; 6. frequently usage of herbal, hypnotics, sedative, stabilizers, or other addictive medication; 7. alcoholics, psychotic, or participants who cannot follow prescription order; 8. heart, respiratory failure, severe diseases; 9. skin disease that may interfere with evaluation of psoriasis, or life-threatening skin disease, history of severe skin disease other than psoriasis; 10. systemic therapy of GC within 2 weeks of screening; 11. topical therapy of group I GC within2 weeks of screening; 12. any systemic therapy for psoriasis (including herbal, chinese medicine) within 4 weeks of screening; 13. any topical therapy for psoriasis (including herbal, chinese medicine).

Design outcomes

Primary

MeasureTime frame
pasi improvement;

Secondary

MeasureTime frame
pasi 50;pga improvement;pasi score;DLQI score;DLQI improvement;pga score;relapse rate;exacerbation rate;

Countries

China

Contacts

Public ContactJie Zheng
jie-zheng2001@126.com+86 18917762309

Outcome results

None listed

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