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Keto Diet vs Standard Cancer Diet for Glioblastoma
Phase 2
Recruiting
Led By Jethro Hu, MD
Research Sponsored by Cedars-Sinai Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up from baseline to 18 months
Summary
This trial is researching whether a Keto Diet could improve survival in glioblastoma patients.
Who is the study for?
This trial is for adults over 18 with newly diagnosed glioblastoma who haven't started chemotherapy or radiation. They must be able to perform daily activities well (KPS ≥ 70), read and understand English or Spanish, and commit to the study's requirements. Excluded are those with recurrent glioblastoma, certain genetic disorders, high steroid needs, pregnancy/nursing status, other experimental therapies, comorbidities that limit participation as per investigator's opinion, electronic medical implants unsafe for MRIs (with some exceptions), BMI < 21kg/m2 unless deemed safe by the investigator.
What is being tested?
The study compares two diets in patients with glioblastoma: a Keto Diet versus a Standard Anti-Cancer Diet. Each participant will also receive standard cancer treatments alongside their assigned diet. The Keto Diet group will have an 18-week intervention monitored by research dietitians through daily ketone and glucose level checks.
What are the potential side effects?
Potential side effects from the Keto Diet may include fatigue, constipation or diarrhea due to dietary changes, low blood sugar levels (hypoglycemia), nutrient deficiencies if not properly managed and possible increase in cholesterol levels.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ from baseline to 18 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from baseline to 18 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Overall survival
Secondary study objectives
Cognitive performance 1
Cognitive performance 2
Health-related quality of life 1
+3 moreTrial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Keto-DietExperimental Treatment1 Intervention
Intensive 18-week Keto Diet intervention.
Group II: Standard Anti-Cancer DietPlacebo Group1 Intervention
Standard Anti-Cancer Diet with Dietitian support
Find a Location
Who is running the clinical trial?
National Cancer Institute (NCI)NIH
13,917 Previous Clinical Trials
41,014,295 Total Patients Enrolled
330 Trials studying Glioblastoma
23,206 Patients Enrolled for Glioblastoma
Cedars-Sinai Medical CenterLead Sponsor
511 Previous Clinical Trials
163,134 Total Patients Enrolled
5 Trials studying Glioblastoma
125 Patients Enrolled for Glioblastoma
Jethro Hu, MDPrincipal InvestigatorCedars-Sinai Medical Center
2 Previous Clinical Trials
60 Total Patients Enrolled
2 Trials studying Glioblastoma
60 Patients Enrolled for Glioblastoma
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have a genetic disorder that affects how my body processes fats.I cannot reduce my steroid dose below 8mg of dexamethasone or its equivalent per day.My glioblastoma has come back after treatment.I am 18 years old or older.I was diagnosed with glioblastoma less than 2 months ago.I haven't started treatment for glioblastoma yet.I am currently on an experimental treatment, but off-label use is okay.I am mostly able to care for myself.
Research Study Groups:
This trial has the following groups:- Group 1: Standard Anti-Cancer Diet
- Group 2: Keto-Diet
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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