Suspendido

The Effect of Plant Phenolic Compounds on Human Colon Epithelial Cells

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

curcumin

+ rutin

+ quercetin

Suplemento DietéticoMedicamento
Quiénes están siendo reclutados

Enfermedades del colon+9

+ Enfermedades del Sistema Digestivo

+ Neoplasias del sistema digestivo

A partir de 18 años
Ver todos los criterios de elegibilidad
Cómo está diseñado el estudio

Estudio de Prevención

Intervencional
Inicio del estudio: agosto de 1996
Ver detalles del protocolo

Resumen

Patrocinador PrincipalUniversity of Medicine and Dentistry of New Jersey
Última actualización: 27 de enero de 2011
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Fecha de inicio: 1 de agosto de 1996

Fecha en la que se inscribió al primer participante.

OBJECTIVES: Determine the response of the colonic epithelium in normal volunteers at average or above average risk of colon cancer, when given short term treatment with plant phenolics such as curcumin, rutin, and quercetin. Compare the colonic mucosal response to the plant phenolics with their response to sulindac in order to evaluate whether they share common mechanisms for colon cancer chemoprevention. Determine the lowest optimal dose for each of the three plant phenolics that is effective in modulating biomarkers of colon epithelial cell turnover and, therefore, potentially inhibiting colon cancer development. Assess the response of the colonic epithelium to curcumin in volunteers at average risk of colon cancer development. OUTLINE: This is a randomized, controlled, two part, single institution study. Patients in Part B are randomized by gender. All patients undergo flexible sigmoidoscopic exam. Part A: Patients, in cohorts of 5-10, receive one of the following five treatments in addition to the control diet: nothing (arm I), oral sulindac twice a day (arm II), oral rutin at 1 of 3 doses twice a day (arms III, IV, and V), oral quercetin at 1 of 3 doses twice a day (arms V, VI, and VII), or at 1 of 3 doses oral curcumin twice a day (arms VIII, IX, and X). Patients are first randomized to the highest doses of rutin, quercetin, and curcumin and then lower doses may be given in order to determine the minimally effective dose. Treatment is continued for 6-10 weeks. Part B: Patients are randomized to receive the control diet only (arm I) or the control diet plus oral curcumin twice a day (arm II) for 6-10 weeks. Patients are followed every 2 weeks. PROJECTED ACCRUAL: There will be 130 patients (110 in Part A and 20 in Part B) accrued into this study.

NCT00003365
Patrocinador PrincipalUniversity of Medicine and Dentistry of New Jersey
Última actualización: 27 de enero de 2011
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.

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.

A partir de 18 años

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

Voluntarios sanos no permitidos

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

Condiciones

Patología

Enfermedades del colonEnfermedades del Sistema DigestivoNeoplasias del sistema digestivoEnfermedades GastrointestinalesNeoplasias GastrointestinalesEnfermedades IntestinalesNeoplasias IntestinalesNeoplasiasNeoplasias por SitioEnfermedades RectalesNeoplasias del ColonNeoplasias colorrectales

Criterios

DISEASE CHARACTERISTICS: Individuals at average risk (Parts A and B) or above average risk (Part A only) for development of colon cancer Average risk individuals defined as: No history of colon adenomas No strong family history of colon polyps or cancer Above average risk individuals defined as: History of one or more sporadic adenomatous polyps at least 0.5 cm in size (either tubular, tubulovillous, or villous adenomas) Have had polypectomy or refused this procedure No significant family history of adenomatous polyps, colon cancer, or hereditary nonpolyposis colorectal cancer or other hereditary colon cancer syndrome Polyps should not have had a focus of adenocarcinoma within them No history of gastrointestinal cancer outside of the large bowel No other gastrointestinal mucosal epithelial disease (e.g., Barrett's esophagus, chronic or recurrent peptic ulcer disease, celiac sprue, or other disorders of nutrient absorption) No significant asymptomatic lesions on flexible sigmoidoscopy, such as inflammation, premalignancy or malignancy PATIENT CHARACTERISTICS: Age: 18 and over Performance status: Not specified Life expectancy: Not specified Hematopoietic: No platelet or coagulation abnormalities No personal or family history of a bleeding disorder Hematopoietic concentration must not be due to significant acute or chronic disorder Hepatic: No liver disease Renal: No renal insufficiency Cardiovascular: No uncontrolled hypertension No chronic congestive heart failure No history of endocarditis No history of rheumatic fever No cardiac valve prostheses No mitral valve prolapse that requires antibiotic prophylaxis Other: HIV negative No gout No pancreatitis No other chronic viral infection No significant acute or uncontrolled chronic medical illness Generally non-smoking (no more than 4 cigarettes per week, i.e., not daily smokers) Must abstain from smoking for at least 1 month prior to enrolling in the study No alcohol consumption of greater than 2 glasses of wine or beer per day Normal weight (90-120% of optimum body weight) and body habitus No change in weight within 5-10% of body weight within the past year No history of inflammatory bowel disease (either ulcerative colitis or Crohn's disease ) No hearing or equilibrium disorders No other prior malignancy except resected carcinoma in situ of the cervix or nonmelanoma skin cancer No allergies to sulindac or tartrazine dyes or prior severe adverse reactions to nonsteroidal antiinflammatory drugs (asthma, gastrointestinal bleeding, or renal insufficiency) No potential allergy to curcumin, quercetin, or rutin No gastrointestinal bleeding Not institutionalized, mentally disabled, or incarcerated No unusually high intake of stored micronutrients or high doses of supplemental calcium or folate Not pregnant or nursing PRIOR CONCURRENT THERAPY: Biologic therapy: Not specified Chemotherapy: Not specified Endocrine therapy: Not specified Radiotherapy: Not specified Surgery: Not specified Other: No concurrent coumadin No chronic use of nonsteroidal antiinflammatory drugs (unless they can be stopped for 3 months) No other putative colon cancer chemoprevention agents (unless they can be stopped for 3 months)

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

Rockefeller University Hospital

New York, United StatesAbrir Rockefeller University Hospital en Google Maps
Suspendido1 Centros de Estudio