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Spots Global Cancer Trial Database for Feasibility Trial of the Modified Atkins Diet and Bevacizumab for Recurrent Glioblastoma

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Feasibility Trial of the Modified Atkins Diet and Bevacizumab for Recurrent Glioblastoma

Official Title: A Feasibility Trial of the Modified Atkins Diet and Bevacizumab for Recurrent Glioblastoma

Study ID: NCT02768389

Study Description

Brief Summary: Patients may participate in this research study if they have glioblastoma. (a brain tumor) that has come back after being treated. Standard treatment for this cancer is a chemotherapy drug called bevacizumab. This research study involves bevacizumab in combination with a special diet called the Modified Atkins Diet (MAD). The purpose of this study is to research if patients can stay on the MAD when it is added to the standard bevacizumab treatment.

Detailed Description: Primary Objective - Determine compliance to treatment at 6 and 12 weeks. Compliance is assessed by review of the daily food diary and the urine and serum ketone levels. Diet compliance is defined as following the diet guidelines 80% of the time with resultant ketosis 80% of the time. If 60% of the patients are compliant with the diet, as defined above, that is a considered a positive result. Secondary Objective(s) * Determine patient compliance in monitoring of blood glucose and urine levels of ketosis. * Determine obstacles to compliance. * Determine the frequency of achieving ketosis, as measured by urine ketones checked daily and serum BHB checked every two weeks. * Determine quality of life (FACT-BR) and adverse events. * Determine response, progression free survival at 6 months (PFS 6), and overall survival (OS). Exploratory Objective * To correlate levels of ketosis and blood sugar with treatment outcome. * To correlate the level of MCT4 expression and IDH1 mutation status with treatment outcome.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University of Cincinnati, Cincinnati, Ohio, United States

University Hospitals Cleveland Medical Center, Seidman Cancer Center, Case Comprehensive Cancer Center, Cleveland, Ohio, United States

Cleveland Clinic Taussig Cancer Institute, Case Comprehensive cancer Center, Cleveland, Ohio, United States

OhioHealth Research and Innovation Institute, Columbus, Ohio, United States

Contact Details

Name: Lisa Rogers, DO

Affiliation: University Hospitals Cleveland Medical Center, Seidman Cancer Center, Case Comprehensive Cancer Center

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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