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

W

Women's Hospital School Of Medicine Zhejiang University

Status

Enrolling

Conditions

Endometrial Cancer Stage I
Endometrial Hyperplasia

Treatments

Drug: Megestrol Acetate 40 MG

Study type

Interventional

Funder types

Other

Identifiers

NCT06417736
PRO2023-3614

Details and patient eligibility

About

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

Enrollment

75 estimated patients

Sex

Female

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 1.18-45 years old with a strong desire to preserve fertility; 2. pathologically diagnosed with primary grade1 or grade2 endometrioid endometrial carcinoma and hyperplasia 3.no signs of suspicious myometrial invasion by enhanced magnetic resonance imaging (MRI) 4. no signs of suspicious extrauterine metastasis by enhanced computed tomography and CT scan of the Lungs

Exclusion criteria

  • 1.have contraindication for pregnancy. 2.no fertility requiremen 3.have myometrial invasion or extrauterine metastasis 4.pathologically diagnosed with primary grade3 endometrioid endometrial carcinoma or non-endometrioid endometrial carcinoma 5.Any disease or symptom that may affect the implementation of the study or the interpretation of the results

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

75 participants in 1 patient group

membrane-inhibiting formula combined with oral progestins
Experimental group
Description:
Megestrol acetate(160mg/day) and membrane-inhibiting formula, 24weeks
Treatment:
Drug: Megestrol Acetate 40 MG

Trial contacts and locations

1

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Central trial contact

Yang Li, Doctor

Data sourced from clinicaltrials.gov

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