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Efficacy and Safety of Weekend Topical Mild Corticosteroid Therapy for Maintenance of Seborrheic Dermatitis: A Randomized Controlled Trial

"Efficacy and Safety of Weekend Topical Mild Corticosteroid Therapy for Maintenance of Seborrheic Dermatitis patients: A Randomized Controlled Trial"

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12625001406493
Enrollment
25
Registered
2025-12-15
Start date
2025-09-01
Completion date
2025-12-31
Last updated
2026-01-05

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

Conditions

None listed

Brief summary

This study aims to determine whether applying a mild corticosteroid cream only on weekends can help prevent flare-ups of seborrheic dermatitis, a common skin condition that affects the face and scalp. After a short treatment to bring the condition under control, participants will be randomly assigned to either continue using the corticosteroid lotion on weekends, along with antifungal shampoo 2/3 times per week or just using antifungal shampoo 2/3 times per week. The study will monitor how long it takes for symptoms to return, and assess quality of life, treatment satisfaction, and any side effects. The researchers believe that weekend-only use of steroid lotion may be effective in maintaining remission with fewer side effects.

Interventions

Arm 1 – Intervention Group: Weekend Topical Corticosteroid Brief name: Weekend topical corticosteroid therapy (mometasone furoate 0.1%) Materials: Mometasone furoate 0.1% lotion (International Non-proprietary Name). Participants will be provided with labeled tubes of the lotion and written instructions for application. Procedures/Activities: Participants first undergo a 2-week induction phase using mometasone furoate 0.1% lotion applied twice daily to affected facial and/or scalp area (1-1.5 F

Arm 1 – Intervention Group: Weekend Topical Corticosteroid Brief name: Weekend topical corticosteroid therapy (mometasone furoate 0.1%) Materials: Mometasone furoate 0.1% lotion (International Non-proprietary Name). Participants will be provided with labeled tubes of the lotion and written instructions for application. Procedures/Activities: Participants first undergo a 2-week induction phase using mometasone furoate 0.1% lotion applied twice daily to affected facial and/or scalp area (1-1.5 Finger tip units for face, 3-4 Finger tip units for scalp), along with antifungal shampoo 2 to 3 times weekly ( every 2nd or 3rd day), to achieve remission. the induction phase can be extended from 2 weeks until there is remission. Upon achieving remission, participants enter the maintenance phase, during which they apply mometasone furoate 0.1% lotion twice per day on weekends ( Saturday and Sunday) to previously affected areas (1-1.5 FTUs for face, 3-4 FTUs for scalp) along with using antifungal shampoo 2 to 3 times weekly9 every 2nd or 3rd day). Provider: Self-administered by participants at home, following training and written instructions provided by dermatology clinic staff. Mode of Delivery: Self-application, individually, at home. Schedule and Duration: Maintenance treatment is delivered twice weekly for 12–24 weeks. Participants remain in the study for a minimum of 12 weeks, and up to 24 weeks if remission is sustained and follow-up monitoring is required. Follow-up visits are scheduled every 4 weeks at the dermatology clinic Each application is twice per day on weekends (Saturday and Sunday). Location: Participant’s home; monitored through outpatient dermatology clinics at scheduled follow-up visits (every 4 weeks). Adaptations: No personalization or titration; the same dose and frequency for all participants in the intervention group. Adherence and Fidelity: Assessed through participant self-reporting and tube weight checks at clinic visits. Clinicians will provide reminders and reinforce correct application at each follow-up.

Sponsors

Dr Imdad ullah khan, dermatology ward, khyber teaching hospital, peshawar
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Primary purpose
Treatment

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

Adults aged 18 to 65 years Clinical diagnosis of moderate to severe seborrheic dermatitis involving the face and/or scalp Achieved remission after a 2-week standardized induction with daily topical corticosteroid therapy. Willing to avoid use of other topical or systemic treatments for seborrheic dermatitis during the study period Provided written informed consent

Exclusion criteria

Presence of other inflammatory dermatoses or infections in the target area Use of systemic corticosteroids or immunosuppressants within the past month Known hypersensitivity or allergy to the study drug or its excipients Pregnant or lactating women Immunocompromised status (e.g. HIV infection)

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026