About this trial
To construct a prediction model of progesterone sensitivity in patients with endometrial cancer treated with fertility preservation
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Have a confirmed pathological diagnosis based upon hysteroscopy: atypical endometrial hyperplasia or 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
Disqualifiers
Acute liver disease or liver tumor (benign or malignant) or renal dysfunction
Pregnancy or potential pregnancy
Confirmed diagnosis of any cancer in reproductive system
Acute severe disease such as stroke or heart infarction or a history of thrombosis disease
Trial population
This study focused on young, pre-menopausal patients with atypical endometrial hyperplasia or endometrioid adenocarcinoma diagnosed by hysteroscopic biopsy, who had a strong desire to preserve reproductive function.
Trial design
Other
Other
Treatments tested in this trial
No intervention
Other interventionNo intervention
Treatment groups
Trial outcomes
Primary outcomes
sensitivity
The sensitivity of the prediction model
accuracy
The accuracy of the prediction model
Secondary outcomes
false-negative rate
The false-negative rate of the prediction model
false-positive rate
The false-positive rate of the prediction model
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Peking University People's Hospital
Lead sponsor
Peking University
Collaborator
Beihang University
Collaborator