Actively Recruiting
Weight Loss Management in Endometrial Cancer Survivors
Led by University of Kansas Medical Center · Updated on 2025-10-27
50
Participants Needed
1
Research Sites
288 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study is being done to understand how oncologists can engage a multidisciplinary team to help endometrial cancer survivors with obesity to engage in a weight management program and potentially start a weight loss medication. Obesity often impacts the future health and longevity of early-stage endometrial cancer survivors more than their cancer diagnosis. Patients will be referred to the KUMC OB/Gyn weight management clinic to discuss weight management options. * If patients decide to use medications for weight loss, then the study will collect data from their chart that is recorded as part of routine monitoring for patients on weight loss medications. * If patients decide not to use any medications, the study will monitor physical exam and lab data collected as part of their routine medical care. The study will also try to understand reasons why patients did or did not start using a weight loss medication.
CONDITIONS
Official Title
Weight Loss Management in Endometrial Cancer Survivors
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years or older
- ECOG performance status of 0 to 2
- Body mass index (BMI) of 30 kg/m2 or higher
- Completed surgical staging with no evidence of remaining disease
- Diagnosed with endometrioid endometrial adenocarcinoma, p53 wild type
- Stage 1 endometrial cancer
- Currently undergoing active surveillance with or without brachytherapy
You will not qualify if you...
- Unable to participate in behavioral weight loss programs
- History of stroke, heart attack, end-stage liver disease, or end-stage kidney disease in the past 6 months
- Currently taking a GLP-1 agonist medication
- Currently using insulin
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Kansas Medical Center
Kansas City, Kansas, United States, 66160
Actively Recruiting
Research Team
P
Principal Investigator
CONTACT
C
Co-investigator
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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