A prospective study of the sampling method of tinea capitis under ultraviolet light/dermoscope: a polit study

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2500099485

Enrollment

Unknown

Registered

2025-03-25

Start date

2024-06-25

Completion date

Unknown

Last updated

2025-03-31

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

Conditions

tinea capitis

Interventions

Gold Standard:Fungal culture was positive

Index test:Sen Spe PPV NPV ROC AUC

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients of suspected tinea capitis

Exclusion criteria

Exclusion criteria: Patients who diagnosed with tinea capitis, has taken systematically antifungal drugs or used topical antifungal drugs in previous month ,or undergoing fungal treatment.

Design outcomes

Primary

Measure	Time frame
Sensitivity;Specificity;PPV;NPV;ROC;AUC;	—

Countries

china

Contacts

Public Contactzhao yan

The First People's Hospital of Jingzhou

zy840609@163.com+86 181 6313 8893

Outcome results

None listed

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