Water Fasting and Chemotherapy for Early-stage Breast Cancer

Gut Microbiome, Adverse Effects, and Markers Through MEtabolic Reprogramming

Recruiting N/A Interventional Study
Breast Cancer Early-stage Breast Cancer
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Female
Study type
Interventional
Purpose
Other
Participants needed
30 (estimated)
Sponsor
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins · Other
Who this trial is looking for

This trial is looking for women with early-stage breast cancer who are planning to receive chemotherapy. Participants will fast for 24-48 hours to see if it helps the treatment work better.

Are You a Good Fit for This Trial?
Must not be taking AllopurinolAspirinAmiodaroneBaclofenBromocriptineCarvedilol
Rules you out End stage renal disease on dialysisCirrhosisUncontrolled hypertensionSeizure disorderHistory of bariatric surgery

You may be able to join if

  • I have been diagnosed with invasive breast cancer stage I-III.
  • I am planning to receive chemotherapy for 4 cycles.
  • I have a BMI of 19.5 or higher.
  • I am willing to change my diet.
  • I can provide stool samples three times during the study.

You may not be able to join if

  • My BMI is below 19.5.
  • I have diabetes.
  • I have a history of eating disorders.
  • I have a serious medical condition.
  • I am pregnant or nursing.
  • I take medications that must be taken with food.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.

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About This Trial

This research is being done to test the feasibility of 24-48 hours of water-only fasting to improve delivery of 4 cycles of chemotherapy in those receiving breast cancer treatment either before or after surgery.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Diagnosed with histologically-confirmed stage I-III invasive carcinoma of the breast * Planning for standard neoadjuvant or adjuvant chemotherapy ddAC or TC for 4 cycles (concurrent anti-HER2 therapy is permitted) * Provider physical exam within 4 weeks of consent * Eastern Co…
Contacts

Jennifer Sheng, MD

202-537-4000

jsheng7@jhmi.edu

CONTACT