C54.1
Conditions
Interventions
Group 1: This is a retrospective data analysis of patient data generated in routine clinical practice from patients who were treated between 2020 and 2025 at the Department of Gynecology and Gynecolog
Sponsors
Klinik für Gynäkologie und gynäkologische Onkologie
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Diagnosed with endometrial cancer
Exclusion criteria
Exclusion criteria: Patients with diagnosed Carcinosarcoma
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is the investigation of the tumor stage and symptoms—particularly postmenopausal/atypical bleeding—at the time of initial diagnosis in patients with endometrial carcinoma, depending on the respective molecular subtype. The data were generated in routine clinical practice and are already fully available prior to the start of the analysis. | — |
Secondary
| Measure | Time frame |
|---|---|
| Currently, there is no defined secondary endpoint. This may change depending on the available data, and will of course be adjusted accordingly if necessary. | — |
Countries
Germany
Contacts
Public ContactLucia Otten
Klinik für Gynäkologie und gynäkologische Onkologie
Outcome results
None listed