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Study identifier: NCT06417736 Synced from ClinicalTrials.gov · July 29, 2026
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Prospective Study for Endometrial Carcinoma and Hyperplasia in Childbearing-age Women

Condition: Endometrial Cancer Stage I · Endometrial Hyperplasia  ·  Sponsor: Women's Hospital School Of Medicine Zhejiang University

PhaseNA
Planned participants75
Who can joinFemale, 18 Years to 45 Years
Healthy volunteersNo

About this study

The goal of this clinical trial is to evaluate the effect and adverse side effects of membrane-inhibiting formula plus oral progestins as fertility-preserving treatment in patients with early-stage endometrial cancer and endometrial hyperplasia research questions:When taken with oral progestins, does the drug membrane-inhibiting formula shorten the time required for complete endometrial remission? What medical problems do participants have when taking drug membrane-inhibiting formula plus oral progestins? Efficacy, side effects, recurrence, pregnancy, and time to obtain pregnancy in different molecular classifications of POLE-mutated, mismatch repair-deficient(MMRd), p53 wild type(p53wt), and p53-abnormal(p53abn). Participants will: Take drug membrane-inhibiting formula plus oral progestins every day Visit the clinic once every 3 months for checkups, tests, and hysteroscopy Keep a diary of examination results and pathology

This description comes directly from the study's public registry record.

Talk to the study team

Yang Li, Doctor  ·  0086-18268165386  ·  5516015@zju.edu.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Women's Hospital School of Medicine Zhejiang UniversityHangzhou, Zhejiang, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06417736