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Recruiting NCT06169449

NCT06169449 Weight Management in Overweight Endometrial Cancer Patients Undergoing Fertility-sparing Treatment

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Clinical Trial Summary
NCT ID NCT06169449
Status Recruiting
Phase
Sponsor Peking University People's Hospital
Condition Endometrium Cancer
Study Type INTERVENTIONAL
Enrollment 240 participants
Start Date 2022-04-01
Primary Completion 2026-12-31

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Weight management--dietWeight management--exerciseWeight management--accompany

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 240 participants in total. It began in 2022-04-01 with a primary completion date of 2026-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: * age ≥18 years old * diagnosed as endometrial cancer or atypical hyperplasia * immunohistochemical staining and sequencing of pathological tissue * fertility-preserving therapy * BMI≥25 kg/m2 * informed consent. Exclusion Criteria: * those with communication barriers * pregnant women * medical and surgical serious complications: urinary calculi, history of renal failure or severe renal insufficiency, familial dyslipidemia, severe liver disease, chronic metabolic acidosis, history of pancreatitis, severe diabetes mellitus, active gallbladder disease, fat dyspepsia, severe cardiovascular and cerebrovascular diseases.

Contact & Investigator

Central Contact

Xiaodan Li, Master

✉ lxd_2000_510@163.com

📞 +8615010305099

Principal Investigator

Xiaodan Li, Master

STUDY CHAIR

Peking University People's Hospital

Frequently Asked Questions

Who can join the NCT06169449 clinical trial?

This trial is open to female participants only, aged 18 Years or older, studying Endometrium Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06169449 currently recruiting?

Yes, NCT06169449 is actively recruiting participants. Contact the research team at lxd_2000_510@163.com for enrollment information.

Where is the NCT06169449 trial being conducted?

This trial is being conducted at Beijing, China.

Who is sponsoring the NCT06169449 clinical trial?

NCT06169449 is sponsored by Peking University People's Hospital. The principal investigator is Xiaodan Li, Master at Peking University People's Hospital. The trial plans to enroll 240 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology