Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT06169449

Weight Management in Overweight Endometrial Cancer Patients Undergoing Fertility-sparing Treatment

Led by Peking University People's Hospital · Updated on 2025-09-03

240

Participants Needed

1

Research Sites

247 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

In this study, overweight and obese patients with endometrial cancer treated with fertility- sparing therapy were randomly divided into two groups. The test group was given weight management, while the control group was given routine care. Relevant information such as body morphology and composition, glycolipid metabolism, molecular typing and tumor outcomes of the subjects were collected. By evaluating the tumor outcome and changes in glycolipid metabolism indicators, to confirm the effectiveness and safety of weight management for overweight and obese patients with endometrial cancer and treatd with fertility preservation.

CONDITIONS

Official Title

Weight Management in Overweight Endometrial Cancer Patients Undergoing Fertility-sparing Treatment

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Diagnosed with endometrial cancer or atypical hyperplasia
  • Immunohistochemical staining and sequencing of pathological tissue performed
  • Currently receiving fertility-preserving therapy
  • Body mass index (BMI) of 25 kg/m2 or higher
  • Provided informed consent to participate
Not Eligible

You will not qualify if you...

  • Communication barriers preventing participation
  • Pregnant women
  • Serious medical or surgical complications such as urinary stones, history of renal failure or severe kidney problems, familial dyslipidemia, severe liver disease, chronic metabolic acidosis, history of pancreatitis, severe diabetes, active gallbladder disease, fat digestion disorders, or severe cardiovascular or cerebrovascular diseases

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Peking University People's Hospital

Beijing, China, China, 100044

Actively Recruiting

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Research Team

X

Xiaodan Li, Master

CONTACT

Y

Yiqian Chen, Master

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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