Prospective Study for Endometrial Carcinoma and Hyperplasia in Childbearing-age Women

Recruiting now · Not applicable

Conditions studied: Endometrial Cancer Stage I, Endometrial Hyperplasia

In brief

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

Key facts

Study ID
NCT06417736
Run by
Women's Hospital School Of Medicine Zhejiang University
People needed
75
Starts
2023-12-01
Expected to finish
2026-12-31
Last updated by the study team
2024-05-16

Who can join

Age: 18 and older, up to 45. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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