Actively Recruiting

Phase 2
Age: 17Years - 45Years
FEMALE
NCT06102863

Progesterone Therapeutic Regimen Plus Statins in Young Women With Early Endometrial Carcinoma and Atypical Endometrial Hyperplasia

Led by Peking University People's Hospital · Updated on 2025-04-29

38

Participants Needed

1

Research Sites

126 weeks

Total Duration

On this page

Sponsors

P

Peking University People's Hospital

Lead Sponsor

B

Beihang University

Collaborating Sponsor

AI-Summary

What this Trial Is About

To explore the treatment efficacy of Progesterone Therapeutic Regimen Plus Statins in patients with atypical endometrial hyperplasia (AEH) and early endometrial carcinoma (EEC) for conservative treatment.

CONDITIONS

Official Title

Progesterone Therapeutic Regimen Plus Statins in Young Women With Early Endometrial Carcinoma and Atypical Endometrial Hyperplasia

Who Can Participate

Age: 17Years - 45Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with atypical endometrial hyperplasia or highly differentiated endometrioid adenocarcinoma stage IA without deep muscle infiltration, cervical involvement, or extrauterine metastasis
  • Strong desire to preserve reproductive function
  • Female patients aged 45 years or younger
  • Patients predicted to be progesterone resistant by a sensitivity prediction model
  • Provided informed consent
  • Willing and able to attend follow-up visits
  • Patients with normal or abnormal blood lipids who have not taken any lipid-lowering drugs
  • Newly treated patients or those with persistent lesions after 12 weeks or partial remission after 24 weeks of prior treatment
Not Eligible

You will not qualify if you...

  • Severe internal diseases or significant liver and kidney impairment
  • Disease progression or extrauterine metastasis during treatment
  • Allergies or contraindications to therapeutic drugs
  • Other types of endometrial cancer or malignant tumors of the reproductive system
  • Breast cancer or other hormone-dependent tumors that prevent progesterone use
  • History of deep vein thrombosis, stroke, or myocardial infarction during treatment
  • Alcohol consumption over 20 grams per day
  • Smoking more than 15 cigarettes per day

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Peking University People's Hospital

Beijing, Beijing Municipality, China, 100044

Actively Recruiting

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Research Team

J

Jianliu Wang, professor

CONTACT

H

HE YIJIAO, PHD/MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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