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NCT07622901Recruiting

Fasting InTervention for Endometrial Cancer

Fasting InTervention for Endometrial Cancer (FIT-ENDO)

Source: ClinicalTrials.gov · Last updated 14 Jul 2026

Brief summary (registry, in English)

The goal of this study is to find out if it is safe for women with endometrial cancer who are going to have surgery to fast (not eat) overnight. Studies have shown that women with endometrial cancer often have problems with metabolism, like high blood sugar. These problems can cause inflammation and may help cancer grow or make treatment less effective. Early research shows that fasting overnight might help improve these problems.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
42 (estimated)
First submitted
20 Mar 2026
Start date
27 Feb 2026
Primary completion date
28 Feb 2028
Lead sponsor
University of Miami
NCT number
NCT07622901

What you commit to

  • Study type: Interventional
  • Planned participants: 42
  • From 27 Feb 2026 to the primary completion date, 28 Feb 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • History of prior hysterectomy.
  • Diagnosis of diabetes treated with insulin, metformin, sulfonylureas, or Glucagon-like peptide-1 (GLP-1) agonist medications.

Other illness

  • Presence of a severe medical or psychiatric condition or medication that would preclude participation of the study intervention, unstable cardiac disease.
  • Recent history of a clinical eating disorder as determined by self-report, medical history, or clinical judgement. Participants with a history of an eating disorder that is well-managed and in sustained remission may be eligible, subject to investigator discretion.
  • Women for whom definitive hysterectomy is not planned for treatment of their endometrial cancer.

Age

  • Women less than 18 years of age.

Other

  • Unable to provide consent.
  • Unable to read/understand English or Spanish.
  • Any contraindication for prolonged overnight fasting of 13 hours or exercising as determined by a physician.
  • Engaging in structured fasting consistently (equal to or more than 50% of the time) for \>12 hours/night.

Who the study is looking for

  • Women 18 years of age or older.
  • Able to provide consent.
  • Able to read/understand English, Spanish or Haitian Creole.
  • Have a diagnosis of Type I (low-grade) endometrial cancer at any stage, histologically confirmed prior to the start of the intervention.
  • Planned minimally invasive surgical treatment (laparoscopy or robotic approach to hysterectomy).
  • Approval to participate from treating oncologist, confirmed via email or in writing.
  • Eastern Cooperative Oncology Group (ECOG) Performance status grade 0-2.
  • Surgeries must be at one of the following institutions:
    • Sylvester Comprehensive Cancer Center
    • University of Miami Hospital (UHealth) Tower
  • Internet access on a smart phone, tablet, or computer.
  • Agree to be randomly assigned to any study group.

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Miami
Coordinator of this site? Confirm its status
MiamiUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.