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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

About this study

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.

Based on ClinicalTrials.gov records.

What participants do

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

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low8%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

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