- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07595133
A Multicenter Clinical Study of Romiplostim N01 in the Treatment of Sepsis-related Thrombocytopenia (ITJ(QN)2510)
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 1
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Qian Wu
- Número de teléfono: +86 13535056114
- Correo electrónico: 295022395@qq.com
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Age ≥ 18 years old, gender unrestricted.
- Meeting the diagnostic criteria of sepsis 3.0, namely: a) confirmed or suspected infection; b) organ dysfunction caused by infection, that is, Sequential Organ Failure Assessment (SOFA) score ≥ 2 points. If organ dysfunction is known to exist before infection, that is, the SOFA score is greater than 0 points, then the SOFA score must increase by ≥ 2 points after the infection occurs.
- Platelet count ≤ 50×109/L.
- The subjects must fully understand and be able to comply with the requirements of the research protocol, and voluntarily sign the informed consent form.
Exclusion Criteria:
- Subjects who are allergic to romiplostim N01 or thrombopoietin, or who have previously received romiplostim N01 or thrombopoietin treatment but showed no therapeutic effect.
- Subjects who have undergone cardiopulmonary resuscitation or have end-stage liver or kidney failure.
- Subjects with thrombocytopenia caused by hematological diseases, or with other hypercoagulable state diseases, recent thrombosis, or acute active bleeding.
- Subjects who have participated in other drug clinical studies within one month.
- Subjects who have used anticoagulants or antiplatelet drugs (such as aspirin, clopidogrel, etc.) within three weeks.
- Subjects who have received platelet-raising treatment (such as methylprednisolone, platelet transfusion, intravenous immunoglobulin or TPO antirheumatic drugs) within two weeks.
- Subjects who have received immunomodulatory agent treatment within six months.
- Subjects who have undergone splenectomy within six months.
- Subjects with a history of radiotherapy or chemotherapy for malignant tumors or with advanced malignant tumors.
- Subjects who have previously received allogeneic stem cell transplantation or organ transplantation.
- Subjects with severe cardiovascular and cerebrovascular diseases, severe trauma, major surgery, or other causes of major bleeding.
- Subjects who were transferred out or died within 24 hours of admission (or ICU).
- Subjects with known or suspected immunosuppression history, including invasive opportunistic infection history (such as histoplasmosis, listeriosis, coccidioidomycosis, pneumocystosis, and aspergillosis); or subjects with complex long-term infections.
- Women who are currently pregnant or breastfeeding, or plan to become pregnant or breastfeed during the study; and men whose partners plan to become pregnant during the study.
- Subjects whom the investigator deems unsuitable for participation in this study for any other reason.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Doble
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: treatment group:Administer Romiplostim treatment
Administer Romiplostim treatment.
Romiplostim for injection N01 (specification: 250 μg per vial) is administered subcutaneously, 250 μg, once a week (since the risk of bleeding in patients with sepsis is high and the included patients have a platelet count of < 50 × 109/L, the starting dose is 4 μg/kg as per the instructions), administered on the first day; a saline solution is used as the placebo, and the administration is repeated for 6 days after the first administration, with the same volume as that of Romiplostim.
|
Administer Romiplostim treatment.
Romiplostim for injection N01 (specification: 250 μg per vial) is administered subcutaneously, 250 μg, once a week (since the risk of bleeding in patients with sepsis is high and the included patients have a platelet count of < 50 × 109/L, the starting dose is 4 μg/kg as per the instructions), administered on the first day; a saline solution is used as the placebo, and the administration is repeated for 6 days after the first administration, with the same volume as that of Romiplostim.
|
|
Comparador activo: Administer recombinant human thrombopoietin therapy
Administer recombinant human thrombopoietin therapy. Thrombopoietin injection (specification: 15000 U/mL) is administered subcutaneously, 15000 U each time, once a day, for a continuous period of ≥1 week. If PLT ≥ 100×109/L, the medication is suspended. If PLT ≤ 10×109/L or there is a significant bleeding tendency, machine-processed platelets are transfused and enhanced hemostasis treatment is provided. (Notes: Both groups of patients were informed of the administration frequency and method.) |
Administer recombinant human thrombopoietin therapy. Thrombopoietin injection (specification: 15000 U/mL) is administered subcutaneously, 15000 U each time, once a day, for a continuous period of ≥1 week. If PLT ≥ 100×109/L, the medication is suspended. If PLT ≤ 10×109/L or there is a significant bleeding tendency, machine-processed platelets are transfused and enhanced hemostasis treatment is provided. (Notes: Both groups of patients were informed of the administration frequency and method.) |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
The effective rate of platelet-stimulating treatment after the 7th day
Periodo de tiempo: 7th day
|
The effective rate of platelet-stimulating treatment after the 7th day
|
7th day
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
The time when platelet count first returned to ≥ 100×109/L
Periodo de tiempo: up to 2 weeks
|
The time when platelet count first returned to ≥ 100×109/L
|
up to 2 weeks
|
|
Platelet counts on the 3rd day, 7th day, 9th day, and 14th day
Periodo de tiempo: 3rd day, 7th day, 9th day, and 14th day
|
Platelet counts on the 3rd day, 7th day, 9th day, and 14th day
|
3rd day, 7th day, 9th day, and 14th day
|
|
The mortality rate 28 days after treatment
Periodo de tiempo: 28 days
|
The mortality rate 28 days after treatment
|
28 days
|
Otras medidas de resultado
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
The incidence of bleeding events after treatment
Periodo de tiempo: through study completion, an average of 1 month
|
The incidence of bleeding events after treatment
|
through study completion, an average of 1 month
|
|
Length of stay in the ICU
Periodo de tiempo: through study completion, an average of 1 month
|
Length of stay in the ICU
|
through study completion, an average of 1 month
|
Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- SHTJH-2026015
- 80,000 yuan (Otro número de subvención/financiamiento: Shanghai Tongji Hospital)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
producto fabricado y exportado desde los EE. UU.
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