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Search / Trial NCT04683237

Liraglutide Plus Megestrol Acetate in Endometrial Atypical Hyperplasia

Launched by XIAOJUN CHEN · Dec 23, 2020

Trial Information

Current as of August 30, 2025

Withdrawn

Keywords

ClinConnect Summary

Backgrounds: High-dose progesterone (MA/MPA) or LNG-IUS is the first-line treatment for women with atypical endometrial hyperplasia (AEH) or early endometrioid cancer who want to preserve fertility. About 70-80% of them can achieve complete response (CR) with the median time of 7-8 months. Over 10% of the patients can not achieve CR and choose operation finally. By the way, long-term treatment of progesterone has many side effects. Our previous study showed that overweight (BMI≥25kg/m2) AEH patients had a significantly increased risk of progesterone treatment failure, and the time to achiev...

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • BMI (body mass index) ≥28kg/m2
  • Consent informed and signed
  • Pathologically confirmed as endometrial atypical hyperplasia
  • Have a strong desire to reproduce and ask for fertility preservation or those who insist on keeping the uterus despite no reproductive requirements
  • Have good compliance and follow-up conditions, and patients are willing to follow up in Obstetrics and Gynecology Hospital of Fudan University in time
  • Exclusion Criteria:
  • Diagnosed as type 2 diabetes
  • Diabetic ketoacidosis
  • History of acute pancreatitis
  • Have a history or family history of medullary thyroid carcinoma; multiple endocrine neoplasia syndrome type 2 (MEN2)
  • Combined with severe medical disease or severely impaired liver and kidney function
  • Patients with other types of endometrial cancer or other malignant tumors of the reproductive system; patients with breast cancer or other hormone-dependent tumors that cannot be used with progesterone
  • Those who require hysterectomy or other methods other than conservative treatment with drugs
  • Deep vein thrombosis, stroke, myocardial infarction
  • Smokers (≥15 cigarettes/day)

About Xiaojun Chen

Xiaojun Chen is a dedicated clinical trial sponsor with a robust background in biomedical research and a commitment to advancing healthcare through innovative clinical studies. With a focus on improving patient outcomes, Chen leads initiatives that emphasize rigorous scientific methodology and ethical standards. His expertise spans various therapeutic areas, enabling the development of novel treatments that address unmet medical needs. By fostering collaboration among multidisciplinary teams and leveraging cutting-edge technology, Xiaojun Chen aims to accelerate the translation of research findings into effective clinical solutions.

Locations

Patients applied

0 patients applied

Trial Officials

xiaojun chen

Principal Investigator

Obstetrics & Gynecology Hospital of Fudan University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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