Suspendido

An Open-Labeled Pilot Study of Biomarker Response in Patients With Colorectal Cancer or Endoscopically Non-Resectable Adenomas Following Short-Term Exposure to Metformin Extended Release (ER)

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

Metformin ER

Medicamento
Quiénes están siendo reclutados

Enfermedades del colon+8

+ Enfermedades del Sistema Digestivo

+ Neoplasias del sistema digestivo

De 18 a 75 años
+28 Criterios de eligibilidad
Ver todos los criterios de elegibilidad
Cómo está diseñado el estudio

Fase 1
Intervencional
Inicio del estudio: mayo de 2013
Ver detalles del protocolo

Resumen

Patrocinador PrincipalM.D. Anderson Cancer Center
Última actualización: 18 de noviembre de 2015
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Fecha de inicio: 1 de mayo de 2013

Fecha en la que se inscribió al primer participante.

Study Groups: If you are found to be eligible to take part in this study, you will be randomly assigned (as in the flip of a coin) to 1 of 2 groups. If you are in Group 1, you will receive metformin ER. You will have a 2 in 3 chance of being assigned to Group 1. If you are in Group 2, you will receive no treatment. You will have a 1 in 3 chance of being assigned to Group 2. Study Drug Administration: If you are in Group 1, You will start taking the drug the day after your colonoscopy (or later if your surgery is scheduled to be more than 30 days after the colonoscopy) and will continue to take it until your scheduled surgery (for up to 30 days). During the first week you will take one tablet of metformin-ER by mouth one time each day with food. From the beginning of the second week until your scheduled surgery, you will take two tablets of metformin-ER by mouth one time each day with food. If you have side effects, your dose may be lowered. If you are in Group 2, you will not receive any study drug from the time of your colonoscopy until surgery. Study Visits: On the day of your colonoscopy: Your medical history will be recorded and you will be asked about any drugs you may be taking. You will have a physical exam. Extra tissue samples will be collected during the colonoscopy for routine and biomarker testing. Biomarkers are small pieces of material or substances found in you tissue that may provide information about your condition or the disease. The study staff will call you 1 week after your colonoscopy and ask about your general health and about any side effects you may be having. On the day before surgery or the day of the surgery itself: Your weight will be measured. Blood (about 3 tablespoons) will be drawn for routine tests and for research about the safety of metformin-ER and how it may affect the disease. This routine blood draw will include a pregnancy test if you are able to become pregnant. You will be asked about your general health and about any side effects you may be having. During the surgery, extra tissue samples will be collected for biomarker testing. Length of Study: You will be on study for up to 30 days. You will no longer be able to take the study drug if the disease gets worse, if intolerable side effects occur, or if you are unable to follow study directions. Your participation on the study will be over once you have had the surgery. This is an investigational study. Metformin-ER is FDA approved and commercially available for the treatment of type 2 diabetes. Its use in this study is investigational. Up to 23 patients will take part in this study. All will be enrolled at MD Anderson.

NCT01816659
Patrocinador PrincipalM.D. Anderson Cancer Center
Última actualización: 18 de noviembre de 2015
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 3 pacientes

Número total de participantes que el ensayo clínico espera reclutar.



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 18 a 75 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 colorrectales

Criterios

16 criterios de inclusión requeridos para participar
2.a. CRC that is potentially resectable and not requiring neoadjuvant treatment

2.b. Endoscopically non-resectable adenoma

2.c. Familial Adenomatous Polyposis (FAP) patient that requires colectomy or proctocolectomy

6.a. CRC or adenoma for which the colorectal surgeon requires a preoperative colonoscopy or sigmoidoscopy for any reason, including but not limited to

Mostrar Más Criterios

12 criterios de exclusión impiden participar
A malignancy currently under active therapy

Chronic liver disease or cirrhosis

Current usage of Metformin

Current usage of insulin, sulfonylureas

Mostrar Más Criterios

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

Experimental
Patients randomized to Metformin-ER 500 mg once daily for one week and then escalation to 1000 mg/day for the duration of the trial. The duration of the trial will be from the preoperative endoscopy till the surgery, and should be not less than 10 days and not more than 30 days.

Grupo II

Sin Intervención
Patients will not receive any study drug from the time of colonoscopy until surgery.

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

University of Texas MD Anderson Cancer Center

Houston, United StatesAbrir University of Texas MD Anderson Cancer Center en Google Maps
Suspendido1 Centros de Estudio