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Efficacy and Safety of Biologics Combined with Antifungal Therapy in Patients with Nail Psoriasis and Onychomycosis: A Single-Center Study Based on Real-World Data

Efficacy and Safety of Biologics Combined with Antifungal Therapy in Patients with Nail Psoriasis and Onychomycosis: A Single-Center Study Based on Real-World Data

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500102342
Enrollment
Unknown
Registered
2025-05-13
Start date
2025-02-21
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

Psoriasis

Interventions

Merged fungal disease A:None
Non-merge of fungal disease A:None

Sponsors

Chengdu Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Meets the diagnostic criteria for psoriasis, accompanied by nail damage; 2. Diagnosed with psoriasis or psoriasis combined with onychomycosis through dermatoscopy or fungal microscopy/fungal culture; 3. Meets the indications for biologic therapy and can be followed up for at least 12 months; 4. The subject or the subject's guardian signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. Contraindications related to biologics: (1) Allergy to active ingredients or other components of biologics; (2) Active infections (including active tuberculosis, highly active hepatitis virus infections, active periods of other viral infections, bacterial infections such as sepsis, etc.) and latent tuberculosis infections; (3) Congestive heart failure with a heart function classification of grade III or IV; (4) Merge with severe uncontrolled liver, lung, or kidney diseases; (5) Malignant tumors, excluding basal cell carcinoma of the skin and tumors with a treatment response period of>=10 years; (6) History of demyelinating syndrome or multiple sclerosis in the past; (7) Congenital or acquired immunodeficiency status; 3. Individuals who have previously been allergic to biologics or antifungal drugs; 4. Other factors that the researcher deems unsuitable for inclusion in this experiment.

Design outcomes

Primary

MeasureTime frame
NAPSI Score;

Countries

China

Contacts

Public ContactBin Yin

Chengdu Second People's Hospital

dr.yb@qq.com+86 13981947519

Outcome results

None listed

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