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NCT04491643CompletedPhase 2

Megestrol Acetate Plus Rosuvastatin in Young Women With Early Endometrial Carcinoma

Source: ClinicalTrials.gov · Last updated 11 Aug 2025

Brief summary (registry, in English)

To explore the treatment efficacy of megestrol acetate plus rosuvastatin in patients with early endometrial carcinoma (EEC) seeking for conservative treatment.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
48 (actual)
First submitted
21 Jun 2020
Start date
1 Sept 2020
Primary completion date
11 Aug 2023
Lead sponsor
Fudan University
NCT number
NCT04491643

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 48
  • From 1 Sept 2020 to the primary completion date, 11 Aug 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Under treatment of high-dose progestin therapy more than 1 months in recent 6 months
  • Already diagnosed with hyperlipidemia and using lipid-lowering drugs

Other illness

  • Acute liver disease or liver tumor (benign or malignant) or renal dysfunction
  • Confirmed diagnosis of any cancer in reproductive system
  • Acute severe disease such as stroke or heart infarction or a history of thrombosis disease
  • Hypersensitivity or contradiction for using MA or atorvastatin

Other

  • Pregnancy or potential pregnancy
  • With other factors of reproductive dysfunction;
  • Strong request for uterine removal or other conservative treatment
  • Smoker (\>15 cigarettes a day)
  • Drinker (\>20 grams a day)

Who the study is looking for

  • Have a confirmed pathological diagnosis based upon hysteroscopy: histologically prove well-differentiated EEC G1 without myometrial invasion
  • No signs of suspicious extrauterine involvement on enhanced magnetic resonance imaging (MRI) or enhanced computed tomography (CT) or ultrasound
  • Have a desire for remaining reproductive function or uterus
  • Good compliance with adjunctive treatment and follow-up
  • Abnormal blood lipid. At least meet one of the following five items:
    • Total cholesterol (TC) ≥ 5.2mmol/L (200mg/dL)
    • Low-density lipoprotein cholesterol (LDL-C) ≥ 3.4mmol/L (130mg/dL)
    • Fasting triglycerides (TG) ≥ 1.7mmol/L (150mg/dL)
    • High-density lipoprotein cholesterol (HDL-C) \< 1.03mmol/L (40mg/dL)
    • Apo-lipoprotein-A (Apo-A) \< 1.0g/L

Age in the registry: 18 years to 45 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Obstetrics and Gynecology Hospital, Fudan University
Coordinator of this site? Confirm its status
ShanghaiChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.