Pharmacokinetic Evaluation of Intravenous Ascorbic Acid
IV Vitamin C
+ IV Vitamin C
+ IV Vitamin C
Neoplasias
Estudio de Tratamiento
Resumen
Fecha de inicio: 1 de mayo de 2011
Fecha en la que se inscribió al primer participante.The purpose of this study is to examine what happens when Vitamin C enters into the body, and the speed and ways it travels through the body, and the rate at which it exits the body in the urine. It is also necessary to determine if it is safe to give Intravenous Vitamin C at high doses.
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.Se reclutarán 34 pacientes
Número total de participantes que el ensayo clínico espera reclutar.Estudio de Tratamiento
Elegibilidad
Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.Cualquier sexo
Sexo biológico de los participantes elegibles para inscribirse.A partir de 21 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
Criterios
PART 1 ELIGIBILITY CRITERIA Inclusion: Healthy adults age 21 or older Laboratory: ANC ≥1,500/mm3, Hemoglobin > 8g/dL, platelet ≥ 100,000/mm3, total bilirubin ≤ 1.5 mg/dL, creatinine ≤2.0 mg/dL, transaminase (AST/ALT) ≤2.5X upper limit, urine uric acid < 1,000mg/d, urine pH <6, urine oxalate <60 mg/d. Participants who have no language barrier, are cooperative, and can give informed consent before entering the study after being informed of the medications and procedures to be used in this study may participate. Exclusion: Glucose-6-phosphate-dehydrogenase (G6PD) deficiency History of bleeding disorder History of oxalate renal calculi; urine oxalate level > 60 mg/d at baseline History of iron overload or hemochromatosis Participants with evidence of a significant psychiatric disorder by history/examination that would prevent completion of the study will not be allowed to participate. Co-morbid condition that would affect survival: end stage congestive heart failure, unstable angina, myocardial infarction within 6 weeks of study, uncontrolled blood sugars ≥ 300 mg/dL, participants with known chronic active hepatitis or cirrhosis. Participants who consume an excess of alcohol or abuse drugs (an excess of alcohol is defined as more than four of any one of the following per day: 30mL distilled spirits, 340mL beer, or 120mL wine) will not be allowed. Participants who smoke tobacco products will not be allowed to participate. PART 2 ELIGIBILITY CRITERIA Inclusion: Oncology participants must have histologically or cytologically diagnosed malignancy. The oncology participants must be age 21 or older and screened for eligibility and have study approved by treating oncologist. Oncology participants must be unwilling or ineligible for further radiation or chemotherapy at the time of enrollment into study. Participants must be without evidence of active spinal cord compression and have predicted lifespan of 6-months or more. ECOG Performance Status 0-2 Eastern Cooperative Oncology Group Performance Status Grade 0 = Fully active, able to carry on all pre-disease activities without restriction Grade 1= Restricted in physical strenuous activity but ambulatory and able to carry out work of a light or sedentary nature e.g. light housework, office work Grade 2 = Ambulatory and capable of all self care but unable to carry out any work activities. Up and about more than 50% of waking hours. Laboratory: ANC ≥1,500/mm3, Hemoglobin > 8g/dL, platelet ≥ 100,000/mm3, total bilirubin ≤ 1.5 mg/dL, creatinine ≤2.0 mg/dL, transaminase (AST/ALT) ≤2.5X upper limit, urine uric acid < 1,000mg/d, urine pH <6, urine oxalate <60 mg/d. Participants who have no language barrier, are cooperative, and can give informed consent before entering the study after being informed of the medications and procedures to be used in this study may participate. Exclusion: Glucose-6-phosphate-dehydrogenase (G6PD) deficiency Currently receiving chemotherapy or radiation therapy History of bleeding disorder History of oxalate renal calculi; urine oxalate level > 60 mg/d at baseline History of iron overload or hemochromatosis Participants with evidence of a significant psychiatric disorder by history/examination that would prevent completion of the study will not be allowed to participate. ECOG Performance Status of 3-4 Grade 3 = Capable of only limited self care, confined to bed or chair more than 50% of waking hours. Grade 4 = Completely disabled. Cannot carry on any self care. Totally confined to bed or chair) and in terminal stages of disease. Co-morbid condition that would affect survival: end stage congestive heart failure, unstable angina, myocardial infarction within 6 weeks of study, uncontrolled blood sugars ≥ 300 mg/dL, participants with known chronic active hepatitis or cirrhosis. Those who consume an excess of alcohol or abuse drugs (an excess of alcohol is defined as more than four of any one of the following per day: 30mL distilled spirits, 340mL beer, or 120mL wine) will not be allowed. Those who smoke tobacco products will not be allowed to participate.
Plan de Estudio
Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.2 grupos de intervención están designados en este estudio
0% de probabilidad de ser asignado al grupo placebo
Grupos de Tratamiento
Grupo I
ExperimentalGrupo II
ExperimentalObjetivos 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
University of Kansas Medical Center
Kansas City, United StatesAbrir University of Kansas Medical Center en Google Maps