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Performance of Clinical Metagenomics in Stool and Urine Samples for Unexplained Diseases Diagnostic and Emerging Diseases Surveillance in Immunocompromised Patients (SENTINEL)

18 de mayo de 2026 actualizado por: Assistance Publique - Hôpitaux de Paris
The study is based on the hypothesis that the concomitant use of mNGS in non-invasive samples (stool, urine) could improve the rate of detected pathogens in immunodeficient patients compared with mNGS performed in an invasive reference sample alone (blood, CSF, broncho-alveolar lavage fluid (BAL), tissue).

Descripción general del estudio

Estado

Aún no reclutando

Condiciones

Intervención / Tratamiento

Descripción detallada

Emerging and re-emerging infectious diseases require broad-spectrum diagnostic approaches capable of identifying a wide range of microorganisms without prior assumptions. This challenge is particularly relevant in immunocompromised patients, who are at high risk for opportunistic, atypical, or previously unknown infections. Conventional microbiological methods rely on targeted assays and may fail to detect uncommon or novel pathogens.

Clinical metagenomics based on high-throughput sequencing (metagenomic Next-Generation Sequencing, mNGS) enables unbiased detection of viral, bacterial, fungal, and parasitic genomes directly from clinical samples. At Necker-Enfants Malades Hospital (Paris, France), implementation of a diagnostic mNGS platform between 2019 and 2022 demonstrated a higher diagnostic yield in immunocompromised patients compared with immunocompetent individuals, with particularly high positivity rates in stool samples. These findings support the evaluation of non-invasive samples as complementary diagnostic matrices.

The SENTINEL study aims to assess the diagnostic performance of mNGS performed on non-invasive samples (stool and urine) compared with invasive reference samples (blood, cerebrospinal fluid, bronchoalveolar lavage fluid, or tissue) in immunocompromised pediatric and adult patients with suspected infection. The underlying hypothesis is that adding stool and/or urine mNGS to invasive sample analysis will increase the detection rate of causative or possibly causative pathogens.

In this multicenter study, invasive samples collected as part of standard of care and study-specific stool and urine samples will undergo centralized mNGS analysis. Non-invasive samples will be collected preferably on the same day as the reference sample or within a maximum of five days.

Clinical and laboratory data generated during routine care will be collected at inclusion. Participants will be followed for three months to evaluate the clinical impact of mNGS findings. For pathogens classified as possibly causative, confirmatory analyses will be performed to support causal attribution.

Secondary analyses will examine the detection of emergent or re-emergent pathogens, including previously unknown pathogens, as well as diagnostic performance according to clinical presentation and type of immune deficiency. The impact of non-invasive mNGS results on patient management and the incremental laboratory cost associated with adding stool and urine analyses will also be evaluated.

The study is sponsored by Assistance Publique - Hôpitaux de Paris and funded by the French Ministry of Health and ANRS Emerging Infectious Diseases.

Tipo de estudio

De observación

Inscripción (Estimado)

120

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

  • Nombre: Aminata TRAORE, Project advisor
  • Número de teléfono: +33 01 42 19 27 34
  • Correo electrónico: aminata.traore6@aphp.fr

Copia de seguridad de contactos de estudio

  • Nombre: Jacques FOURGEAUD, PharmD, PhD
  • Número de teléfono: +33 01 44 49 56 11
  • Correo electrónico: jacques.fourgeaud@aphp.fr

Ubicaciones de estudio

    • Île-de-France Region
      • Paris, Île-de-France Region, Francia, 75015
        • Hopital Necker - Enfants Malades
        • Contacto:
          • Aminata TRAORE, Project advisor
          • Número de teléfono: +33 01 42 19 27 34
          • Correo electrónico: aminata.traore6@aphp.fr
        • Contacto:
        • Investigador principal:
          • Jacques FOURGEAUD, PharmD, PhD

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Niño
  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Método de muestreo

Muestra no probabilística

Población de estudio

Pediatric or adult patient with a primary or secondary immune deficiency

Descripción

Inclusion Criteria:

  • Pediatric or adult patient with a primary or secondary immune deficiency (including immunosuppressive therapy, chemotherapy, HIV infection).
  • mNGS prescription on tissue, CSF, BAL and/or blood to identify the causative pathogen in patient with symptoms or biological signs compatible with an infection as per investigator's judgment (e.g., fever, leukocytosis, increased CRP level)
  • Non opposition of the participant (or parent(s)/ legal guardian(s) of infant participant)

Exclusion Criteria:

  • No healthcare insurance

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

Cohortes e Intervenciones

Grupo / Cohorte
Intervención / Tratamiento
Pediatric or adult patient with a primary or secondary immune deficiency
Pediatric or adult populations with a primary or secondary immune deficiency following immunosuppressive treatment or an underlying disease are at increased risk of severe infection by a wide range of viruses.
The intervention aims to increase pathogen detection of mNGS with the addition of non-invasive samples compared with invasive sampling alone

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Detection of a "causative" or "possibly causative" pathogens by mNGS in Non-Invasive (stool and/or urine) and invasive samples (blood, CSF, BAL and/or tissue)
Periodo de tiempo: 14 days
  • Possibly causative pathogen: microorganism associated with the symptoms in literature but without formal proof of causality.
  • Causative pathogen: known pathogen detected and typical associated symptoms.
14 days

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Detection of emergent or re-emergent pathogens by mNGS in non-invasive samples (stool and/or urine) and invasive sample (blood and/or CSF and/or BAL and/or tissue)
Periodo de tiempo: 14 days

Among detected "causative" or "possibly causative" pathogen", evaluation of emergent or re-emergent pathogen:

  • Emergent or re-emergent pathogen: pathogen with no known circulation in the geographical area and during the period in which it will be identified
  • Pathogen X: infectious agent that is not currently known to cause human disease, but an aetiologic agent of a future outbreak with epidemic or pandemic potential.
14 days
Changes in patient management
Periodo de tiempo: 3 months
Evaluation of the impact of stool and urine mNGS results on patient management: administration of antimicrobial therapy and/or specific or polyvalent immunoglobulins, change in the management of immunosuppression (reduction of immunosuppressive therapy, delay of solid organ or haematopoietic stem cell transplantation), hospitalization (incidence, duration) and/or additional samples collection
3 months
Detection of the "possibly causative" pathogen genomes by specific PCR in all available invasive and non-invasive samples collected at inclusion and by in situ hybridization in available tissue sample collected at inclusion
Periodo de tiempo: 14 days
Confirmation of the role of the detected "possibly causative" pathogen in the patient's symptoms using additional investigations.
14 days
Detection of "causative" or "possibly causative" Pathogens by mNGS in Non-Invasive Samples in different subgroups
Periodo de tiempo: 14 days
Subgroups according to symptoms, immune deficiency type and age
14 days
Cost of performing mNGS in invasive, stool and urine samples
Periodo de tiempo: 14 days
Calculation of the cost (including laboratory personnel and reagents) of performing mNGS in invasive, stool and urine samples
14 days

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Colaboradores

Investigadores

  • Investigador principal: Jacques FOURGEAUD, PharmD, PhD, Assistance Publique - Hôpitaux de Paris
  • Silla de estudio: Pierre FRANGE, MD, PhD, Assistance Publique - Hôpitaux de Paris

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

1 de junio de 2026

Finalización primaria (Estimado)

1 de junio de 2028

Finalización del estudio (Estimado)

1 de septiembre de 2028

Fechas de registro del estudio

Enviado por primera vez

18 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

18 de mayo de 2026

Publicado por primera vez (Actual)

22 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

22 de mayo de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

18 de mayo de 2026

Última verificación

1 de mayo de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • APHP241015

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .