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Ketogenic Diet for Skin and Kidney Cancers
N/A
Waitlist Available
Led By Marium Husain, MD, MPH
Research Sponsored by Ohio State University Comprehensive Cancer Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Patients with confirmed diagnosis of metastatic melanoma receiving first line treatment with specified medications
Patients with confirmed diagnosis of metastatic renal cell carcinoma receiving first line treatment with specified medications
Must not have
Individuals < 18 years of age
Patients who are clinically underweight (BMI < 18.5) at the start of treatment
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 1 year
Awards & highlights
No Placebo-Only Group
Summary
"This trial aims to see if following a ketogenic diet, which involves eating fewer carbohydrates and more fats, can improve the response to immunotherapy in patients with metastatic melanoma and kidney cancer. The idea
Who is the study for?
This trial is for patients with metastatic melanoma or kidney cancer. Participants should be eligible for immunotherapy and willing to follow a ketogenic diet, which means eating fewer carbs and more fats.
What is being tested?
The study tests if a ketogenic diet can boost the effectiveness of immune checkpoint inhibitors (a type of immunotherapy) in treating metastatic melanoma and kidney cancer.
What are the potential side effects?
Potential side effects may include those associated with a strict ketogenic diet, such as fatigue, headache, dizziness, nutrient deficiencies, and gastrointestinal discomfort.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have metastatic melanoma and am on my first treatment.
Select...
I have metastatic renal cell carcinoma and am on my first treatment.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am under 18 years old.
Select...
I am underweight with a BMI below 18.5.
Select...
I am not currently in a cancer treatment study.
Select...
I have diabetes and use insulin.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 1 year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 1 year
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Adherence (feasibility measure)
Incidence of adverse events
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Arm I (Ketogenic diet)Experimental Treatment7 Interventions
Patients undergo a ketogenic dietary intervention with personalized coaching from a dietician about the KD, which includes extensive educational and ongoing support on the KD and continuous ketone monitoring by talking to a dietician directly, with the ability to text a dietician at any time and expect a response within 12 hours over 24weeks. Patients also undergo daily blood glucose and ketone monitoring, undergo CT, undergo blood sample collection and may undergo stool sample collection on the study.
Group II: Arm II (usual caare)Active Control1 Intervention
Patients follow a standard of care diet on the study.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Biospecimen Collection
2004
Completed Phase 3
~2020
Computed Tomography
2017
Completed Phase 2
~2740
Find a Location
Who is running the clinical trial?
Ohio State University Comprehensive Cancer CenterLead Sponsor
340 Previous Clinical Trials
294,206 Total Patients Enrolled
1 Trials studying Cutaneous Melanoma
100 Patients Enrolled for Cutaneous Melanoma
Marium Husain, MD, MPHPrincipal InvestigatorOhio State University Comprehensive Cancer Center
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