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An Open-Label, Parallel Comparison Study to Evaluate the Effect of Oral Administration of Nattokinase Taken by Normal Subjects, Patients Under Dialysis, and Patients of Cardiovascular High Risk Groups

0 criterios cumplidosConsulta de un vistazo cómo tu perfil cumple con cada criterio de elegibilidad.
Qué se está evaluando

Colección de datos

Quiénes están siendo reclutados

Enfermedades Cardiovasculares

+ Trombosis

+ Enfermedades Vasculares

De 20 a 70 años
Ver todos los criterios de elegibilidad
Cómo está diseñado el estudio

Estudio de Prevención

Fase 4
Intervencional
Inicio del estudio: junio de 2005
Ver detalles del protocolo

Resumen

Patrocinador PrincipalChanghua Christian Hospital
Última actualización: 27 de enero de 2026
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Fecha de inicio: 1 de junio de 2005

Fecha en la que se inscribió al primer participante.

This study will employ an open-label, parallel-group design. Adult men and women who meet the inclusion/exclusion criteria and give written consent to participate will be assigned to one of the three groups according to their condition: Group A- normal volunteers; Group B- patients under dialysis; Group C- patients of cardiovascular high risk group. Each group will enroll 15 subjects. After two to four weeks run-in period, subjects will be given nattokinase orally for 8 weeks, and will be asked to stop taking nattokinase for 2 weeks to evaluate the effect of long-term intake and cease of intake of nattokinase. Laboratory tests, including fibrinogen, T-PA, PAI-1, D-dimer, total cholesterol, LDL-C, HDL-C, and TG, vital signs and body weight will be evaluated at screening visit, 3 days, 1 week, 4 weeks, 8 weeks, and 10 weeks (2 weeks after cease of intake) visits. Patient self-evaluation of tolerance and physical improvement will be assessed by a Patient Questionnaire at 3-day, and 1-, 4-, 8-, and 10-week visits. Each patient will be carefully monitored for the development of any adverse events (AE).

Título OficialAn Open-Label, Parallel Comparison Study to Evaluate the Effect of Oral Administration of Nattokinase Taken by Normal Subjects, Patients Under Dialysis, and Patients of Cardiovascular High Risk Groups
Patrocinador PrincipalChanghua Christian Hospital
Última actualización: 27 de enero de 2026
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Protocolo

Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.
Detalles del Diseño

Se reclutarán 45 pacientes

Número total de participantes que el ensayo clínico espera reclutar.

Estudio de Prevención

Los estudios de prevención buscan evitar que se desarrolle una enfermedad. A menudo incluyen a personas en riesgo y evalúan vacunas, cambios en el estilo de vida o medicamentos preventivos.


Elegibilidad

Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.
Condiciones
Criterios

Cualquier sexo

Sexo biológico de los participantes elegibles para inscribirse.

De 20 a 70 años

Rango de edades de los participantes que pueden unirse al estudio.

Voluntarios sanos permitidos

Indica si personas sanas, sin la condición que se estudia, pueden participar.

Condiciones

Patología

Enfermedades CardiovascularesTrombosisEnfermedades Vasculares

Criterios

Inclusion Criteria: * In order to be enrolled in the study, potential study subjects must meet the following inclusion criteria: 1. Men and non-pregnant women who are at least 20 and younger than 70 years of age. 2. Subjects who are, in the opinion of the Investigator, able to comply with the requirements of the study. 3. Subjects who have been adequately informed of the nature and risks of the study and who have given written informed consent prior to receiving investigational product. Group-specific inclusions criteria: Group A: 1. Subjects have no risk factors of cardiovascular diseases (see Group C) or chronic renal diseases in the history. 2. Male subjects have Creatinine≦1.4 mg/dl; Female≦1.3 mg/dl. Group B: 1\. Patients have been receiving dialysis at the same institute for at least 3 months. Group C: 1. Patients have coronary artery disease (CAD); OR 2. Patients have peripheral arterial occlusive disease (PAOD); OR 3. Patients have history of stroke; OR 4. Patients have history of transient ischemic attack (TIA); OR 5. Patients have history of pulmonary embolism (PE); OR 6. Patients have history of deep vein thrombosis (DVP); OR 7. Patients have more than 2 major risk factors of cardiovascular disease (CVD) listed by National Health Insurance guidelines such as hypertension, smoking, diabetes mellitus (DM), atrial fibrillation (AF), lipid disorder, overweight, physical inactivity, etc. Exclusion Criteria: * In order to be enrolled in the study, potential study patients must not have any of the following exclusion criteria: 1. Known allergies to the component of study product. 2. Current use of warfarin. 3. Patients have active disease status. 4. Patients have acute disease, and in the opinion of investigators, are not suitable to participate in this study. Group-specific exclusion criteria: Group A: 1. Patients have coronary artery disease (CAD). 2. Patients have peripheral arterial occlusive disease (PAOD). 3. Patients have history of stroke. 4. Patients have history of transient ischemic attack (TIA). 5. Patients have history of pulmonary embolism (PE). 6. Patients have history of deep vein thrombosis (DVP). 7. Patients have more than 2 major risk factors of cardiovascular disease (CVD) listed by National Health Insurance guidelines such as hypertension, smoking, diabetes mellitus (DM), atrial fibrillation (AF), lipid disorder, overweight, physical inactivity, etc. 8. Patients have history of chronic renal diseases. 9. Male subjects have Creatinine\>1.4 mg/dl; Female\>1.3 mg/dl.

Plan de Estudio

Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.
Objetivos del Estudio

Objetivos del Estudio

Objetivos Primarios

Objetivos Secundarios

Centros del Estudio

Estos son los hospitales, clínicas o centros de investigación donde se lleva a cabo el estudio. Puedes encontrar la ubicación más cercana a ti y su estado de reclutamiento.

Este estudio tiene una ubicación

Suspendido

Changhua Christian Hospital

Changhua, TaiwanAbrir Changhua Christian Hospital en Google Maps
Completado1 Centros de Estudio