Completado

Does Protein Restriction Inhibit Prostrate Cancer Growth

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

Protein restrictive diet

Otro
Quiénes están siendo reclutados

Enfermedades Urogenitales+6

+ Enfermedades Genitales

+ Enfermedades Genitales Masculinas

Ver todos los criterios de elegibilidad
Cómo está diseñado el estudio

Estudio de Ciencia Básica

Intervencional
Inicio del estudio: enero de 2011
Ver detalles del protocolo

Resumen

Patrocinador PrincipalWashington University School of Medicine
Última actualización: 26 de marzo de 2021
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Fecha de inicio: 1 de enero de 2011

Fecha en la que se inscribió al primer participante.

The primary objective of this study is to determine whether or not a low protein diet has an inhibitory effect on prostate cancer cell growth. The primary outcome measures relative to the investigators primary objectives are: For Group 1 the expression of genes and proteins of the PI-3K/Akt/mTOR pathway. For Group 2 the PSA values obtained every three months.

Patrocinador PrincipalWashington University School of Medicine
Última actualización: 26 de marzo de 2021
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 65 pacientes

Número total de participantes que el ensayo clínico espera reclutar.

Estudio de Ciencia Básica

Los estudios de ciencia básica ayudan a los investigadores a comprender cómo funciona el cuerpo o cómo se desarrolla una enfermedad. No prueban tratamientos, pero sientan las bases para terapias futuras.



Elegibilidad

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

Hombre

Sexo biológico de los participantes elegibles para inscribirse.

Voluntarios sanos no permitidos

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

Condiciones

Patología

Enfermedades UrogenitalesEnfermedades GenitalesEnfermedades Genitales MasculinasNeoplasias Genitales MasculinasNeoplasiasNeoplasias por SitioEnfermedades ProstáticasNeoplasias UrogenitalesNeoplasias prostáticas

Criterios

Inclusion Criteria: group 1 Patient must have a diagnosis of prostate cancer confirmed by pathology. Patient must be scheduled to undergo radical prostatectomy no sooner than 6 weeks from date of enrollment (to allow for a minimum of 4 weeks on the low protein diet). Patient must have adequate baseline protein intake (screening 4-day food record shows protein > 1.0 g/kg FFM) Patient must be able to understand the English-language instructions. Patient must be able to comply with the low protein diet (as evaluated by the dietitian and other study team members). Patient must be able to understand and willing to sign an IRB-approved written informed consent document. 5.2.2 Inclusion Criteria - Group 2 Patient must have a diagnosis of prostate cancer. Patient must have previously undergone a radical prostatectomy for treatment of prostate cancer. Patient must have a detectable PSA (defined as PSA ≥ 0.1) in at least two consecutive measurements, taken at least one month apart, with no therapy between the PSA measurements. If the patient has had additional therapy after the radical prostatectomy, there must be evidence of a rising PSA (i.e., two consecutive measurements at least one month apart) after the patient has completed the intervening therapy (meaning that the patient must have failed treatment). Patient must have adequate baseline protein intake (screening 4-day food record shows protein > 1.0 g/kg FFM). Patient must have adequate baseline caloric intake (screening 4-day food record shows caloric intake of > 1500 kcal/day). Patient must be able to understand the English-language instructions. Patient must be able to comply with the low protein diet (as evaluated by the dietitian and other study team members). Patient must be able to understand and willing to sign an IRB-approved written informed consent document. Exclusion Criteria: Patient must not currently be receiving any therapy for prostate cancer. Patient must not have any serious chronic illness such as unstable angina, any uncontrolled metabolic disorder, or any immunologic disorder. Patient must not have a history of any previous malignancy (with the exception of squamous or basal cell carcinoma of the skin) in the 5 years prior to enrollment (for Group 1) or 12 months prior to enrollment (for Group 2). Patient must not have a previous history of a stroke. Patient must not be taking any medications that might confound the study results (anabolic agents (such as androgen, androgen precursor, rhGH) in the 6 months prior to enrollment; corticosteroids (other than nasal) in the 6 months prior to enrollment; or finasteride or dutasteride). Patient must not have dementia or any other cognitive impairment. Patient must not have a lifestyle or fixed diet pattern that would interfere with participation in or interpretation of the results of this study -

Plan de Estudio

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

2 grupos de intervención están designados en este estudio

0% de probabilidad de ser asignado al grupo placebo

Grupos de Tratamiento

Grupo I

Sin Intervención
No changes in dietary group

Grupo II

Experimental
reduced protein diet

Objetivos del Estudio

Objetivos Primarios

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

Washington University School of Medicine

St Louis, United StatesAbrir Washington University School of Medicine en Google Maps
Completado1 Centros de Estudio