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Study details
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Fasting During Neoadjuvant Chemotherapy

Case Comprehensive Cancer Center
NCT IDNCT06386887ClinicalTrials.gov data as of Apr 2026
Target enrollment

20

Study length

about 1.5 years

Ages

18+

Sex

Female only

Locations

1 site in OH

What this study is about

This trial is testing whether timed fasting during chemotherapy before surgery can be achieved, safe, and improve quality of life compared to standard dietary recommendations for women with epithelial ovarian cancer. Participants will either follow a fasting schedule or receive regular diet advice while undergoing neoadjuvant chemotherapy.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Participate in Intermittent Fasting
  • 2.Take Neoadjuvant chemotherapy

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
Randomized & Blinded

You may get a placebo/standard care, and you won't know which.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Secondary: Chemotherapy related toxicity at Cycle 2, Chemotherapy related toxicity at Cycle 3, Chemotherapy related toxicity at Cycle 4, Chemotherapy related toxicity at post treatment, Post Quality of Life (QLQ-C30) Score Post Treatment, Pre Quality of Life (QLQ-C30) Score at Baseline

Body systems

Oncology