Can Fasting Decrease the Side Effects of Chemotherapy?
Status unconfirmed · Not applicable
Conditions studied: Chemotherapy Effect, Chemotherapeutic Toxicity, Fasting
In brief
This is a prospective randomized crossover trial. Patients will be randomized to the FMD or regular diet during three rounds of chemotherapy. After the third round, patients will cross over to the opposite arm. The primary hypothesis is that there will be fewer cases of Grade 2-4 nausea when patients are in the FMD sequence. The primary objective is to assess differences in toxicities in patients undergoing chemotherapy with a combination of taxol/carboplatin when using a fasting mimicking diet when compared to normal diet before and after treatment.
Key facts
- Study ID
- NCT04027478
- Run by
- Sutter Health
- People needed
- 39
- Starts
- 2019-09-01
- Expected to finish
- 2021-02-01
- Last updated by the study team
- 2019-07-22
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 18 years of age and older
- English speaking
- Patients undergoing chemotherapy with Taxol/carboplatin planned for at least 6 cycles
- Willing to comply with diet and tests
- No significant medical problem that would make fasting dangerous (insulin dependent diabetes, history of hypoglycemia)
You may not qualify if…
- Insulin dependent diabetes
- Pregnancy
- History of hypoglycemia, or any other medical condition that the treating physician considers not suitable for fasting
Where it is running
- Sutter Cancer Center — Sacramento, California, United States
Full record on ClinicalTrials.gov
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