Viewing Study NCT06417736



Ignite Creation Date: 2024-05-19 @ 5:33 PM
Last Modification Date: 2024-10-26 @ 3:29 PM
Study NCT ID: NCT06417736
Status: RECRUITING
Last Update Posted: 2024-05-16
First Post: 2024-05-12

Brief Title: Prospective Study for Endometrial Carcinoma and Hyperplasia in Childbearing-age Women
Sponsor: Womens Hospital School Of Medicine Zhejiang University
Organization: Womens Hospital School Of Medicine Zhejiang University

Study Overview

Official Title: Prospective Clinical Study of Fertility-sparing Treatment With a Membrane-inhibiting Formula Combined With Oral Progestins for Endometrial Carcinoma and Hyperplasia in Childbearing-age Women
Status: RECRUITING
Status Verified Date: 2023-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: 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 questionsWhen 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-deficientMMRd p53 wild typep53wt and p53-abnormalp53abn

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
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None