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Epidemiological and Molecular Analysis of Scalp Ringworm in France (TCC-France)

1 de junho de 2026 atualizado por: Assistance Publique - Hôpitaux de Paris

Epidemiological and Molecular Analysis of Scalp Ringworm in France With Antifungal Susceptibility Testing: A Multicenter Prospective Study

Ringworm of the scalp or tinea capitis (TC) is the most common fungal infection in children. Few data are currently available in France concerning these infections, either on the distribution of the causative dermatophytes species or on the response to treatment. In addition, following the sudden cessation of the marketing of griseofulvin in March 2021, the only treatment with Marketing Authorization in France in children, the new recommendations recommend oral terbinafine or itraconazole. Yet, resistance of dermatophytes to terbinafine has appeared in France for a few years with recently reported cases of recalcitrant cutaneous dermatophytosis due to Trichophyton spp. imported from the Indian subcontinent. Moreover, the morphological identification of dermatophyte species is not always easy in routine practice, in particular within the T. interdigitale/mentagrophyytes/indotineae and Trichophyton rubrum/soudanense/violaceum complexes, the latter being frequently responsible for TC.

This study therefore aims to describe the epidemiology of TC in France from a clinical point of view, the responsible species and the response to treatment since the recent modification of therapeutic recommendations. To do this, a collection of data and isolates of dermatophytes responsible for TC in 11 French centers will be carried out during the year 2023. Then an epidemiological-molecular analysis of the isolates will be carried out as well as the determination of their sensitivity to antifungals searching for an acquired resistance.

Visão geral do estudo

Status

Concluído

Descrição detalhada

Objectives/Hypotheses The overall objective of this study is to describe the epidemiology of tinea capitis (TC) in France from clinical, species, and treatment response perspectives.

To achieve these objectives, it will be necessary to:

  • Identify isolates using various methods (morphological, proteomic, and molecular),
  • Perform phylogenetic analysis of the isolates,
  • Determine the susceptibility of isolates to four antifungal agents (terbinafine, itraconazole, voriconazole, and ketoconazole),
  • And, in the event that resistant isolates are identified, characterize the mechanisms of resistance to terbinafine and/or azoles.

Methodology Participating Centers Eleven centers (10 university hospitals and one private laboratory) were selected based on the results of two national surveys on TC conducted by the French Society for Medical Mycology (SFMM) between 2014 and 2019. Centers reporting at least 20 cases per year were included, ensuring at least one center per region. The estimated number of cases for 2023 is approximately 635.

The participating centers will be responsible for:

  • Identifying dermatophyte isolates from scalp samples using classical phenotypic methods and/or MALDI-TOF mass spectrometry with the online MSI-2 database (for the 6/11 centers that routinely use this method),
  • Storing isolates in microtubes at -20°C (or sending primary culture tubes monthly for the five Parisian centers) for subsequent shipment to the Parasitology-Mycology Laboratory in Bobigny,
  • Completing part of the data collection form (using a request sheet filled out at the time of sampling, provided as an appendix).

Isolates All dermatophyte isolates obtained from scalp sample cultures in the 11 centers between January 2, 2023, and December 31, 2023, will be studied. After identification using each laboratory's standard techniques, isolates will be stored at -20°C in microtubes (provided) for later shipment to the Parasitology-Mycology Laboratory at Avicenne Hospital. Parisian centers may choose to send primary culture tubes monthly or to store isolates in microtubes at -20°C for later shipment to Avicenne.

Data Collection Form A REDcap collection form will be available online. Isolates will be anonymized using a code for each center, consisting of a three-letter abbreviation for the city or hospital followed by a number (001 to XXX).

Each center will record the following data: local case number, demographic and clinical information, phenotypic identification (with or without MALDI-TOF MS), previous treatments (corticosteroids and/or antifungals), first-line treatment (dose and outcome at one and, if necessary, two months-cure/improvement or need for second-line treatment).

Additional results (MALDI-TOF MS identification, ITS region sequencing, and antifungal susceptibility testing) will be entered by the coordinating center.

Patients will be required to sign a non-opposition form for the use of their demographic, clinical, and biological data for research purposes. All procedures will adhere to the ethical standards of the 1975 Declaration of Helsinki, as revised in 2008.

Isolate Identification Dermatophyte isolates will be identified phenotypically by each center and by MALDI-TOF MS using the online MSI-2 database (https://msi.happy-dev.fr) for centers that already use this method routinely, or by the coordinating center. Molecular identification will also be performed by the coordinating center using PCR-sequencing of ribosomal DNA targeting the ITS1, 5.8S rDNA, and ITS2 regions, as well as the β-tubulin 2 gene (14), following fungal DNA extraction using the Chelex method. The obtained sequences will be aligned with reference sequences from various databases (MycoBank, ISHAM Barcoding, and GenBank).

Phylogenetic Analysis of Isolates A phylogenetic analysis will be performed for the predominant species isolated, presumably T. tonsurans, representing approximately 30-35% of isolates. This analysis will use maximum likelihood methods via MEGA software, based on sequences of the ITS regions and the β-tubulin 2 (BT2) gene. Additional genes such as ALP1, SQLE, and TEF-1α may also be sequenced for multi-locus sequence typing (MLST) analysis (8,15).

Other isolates will be preserved and studied as part of a doctoral thesis, but as an ancillary study to this research project.

Antifungal Susceptibility Testing For non- or poorly sporulating isolates (such as Microsporum audouinii and species within the T. rubrum complex), subculturing on potato dextrose agar supplemented with 20% CO₂ will be performed beforehand to stimulate sporulation (19).

Antifungal susceptibility will be determined for sporulating isolates using three different methods by the coordinating center:

  • Screening for terbinafine-resistant isolates using a terbinafine-containing agar medium (0.2 mg/mL TCAM) (16). Each isolate will be cultured in parallel on RPMI agar plates with and without terbinafine, following an established protocol (A. Sabater-Moreno and E. Dannaoui).
  • Determination of minimum inhibitory concentrations (MICs) using RPMI agar strips for itraconazole (E-test™ strips, BioMérieux) and terbinafine (Ezy MIC™ strips, DMLABO).
  • Determination of MICs for terbinafine, itraconazole, voriconazole, and ketoconazole (Sigma-Aldrich) using the EUCAST method adapted for conidia-producing dermatophytes (17,18). The 50% inhibitory concentration (IC₅₀) will be determined by spectrophotometry. Isolates will be considered at risk of resistance when the IC₅₀ exceeds the Epidemiological Cut-Off Value (ECOFF).

Characterization of Resistance Mechanisms to Terbinafine and Azoles Various antifungal resistance mechanisms have been reported in dermatophytes, including point mutations or alterations in drug targets, as well as increased efflux of antifungals due to overexpression of ABC or MFS transporter genes, or more recently, overexpression of the TinCYP51B gene encoding lanosterol 14α-demethylase, the target of azoles (20-23).

Resistance to terbinafine is primarily associated with modifications in squalene epoxidase (SQLE), an enzyme involved in an early step of membrane ergosterol synthesis and the target of allylamines. If terbinafine-resistant isolates are identified during this study, the SQLE gene will be amplified and sequenced to detect point mutations (Leu393, Phe397, Phe415, and His440) by aligning obtained sequences with reference sequences from various databases (MycoBank, ISHAM Barcoding, and GenBank). If azole-resistant isolates are identified, point mutations in the ERG11 gene encoding sterol 14-α demethylase will be investigated.

Tipo de estudo

Observacional

Inscrição (Real)

701

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

    • Seine Saint Denis
      • Bobigny, Seine Saint Denis, França, 93009
        • Parasitology-Mycology Department, Avicenne Hospital AP-HP,

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Filho
  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Método de amostragem

Amostra Não Probabilística

População do estudo

Patients with tinea capitis (TC) in France

Descrição

Inclusion Criteria:

  • All dermatophyte isolates obtained from scalp sample cultures in the 11 centers between January 2, 2023, and December 31, 2023,

Exclusion Criteria:

-

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Describe the epidemiology of tinea capitis (TC) in France from clinical, species, and treatment response perspectives.
Prazo: Inclusion

To achieve these objectives, it will be necessary to:

  • Identify isolates using various methods (morphological, proteomic, and molecular),
  • Perform phylogenetic analysis of the isolates,
  • Determine the susceptibility of isolates to four antifungal agents (terbinafine, itraconazole, voriconazole, and ketoconazole),
  • And, in the event that resistant isolates are identified, characterize the mechanisms of resistance to terbinafine and/or azoles.
Inclusion

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

2 de janeiro de 2023

Conclusão Primária (Real)

31 de dezembro de 2023

Conclusão do estudo (Real)

31 de dezembro de 2023

Datas de inscrição no estudo

Enviado pela primeira vez

1 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

1 de junho de 2026

Primeira postagem (Real)

8 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

8 de junho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

1 de junho de 2026

Última verificação

1 de maio de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • 2026-550

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

INDECISO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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