A Multi-center Prospective Study on the Oncological and Reproductive Outcomes and Quality of Life in Young Woman After Fertility-sparing Treatment of Endometrial Cancer and Endometrial Intraepithelial Hyperplasia
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Endometrial Cancer, Endometrial Intraepithelial Neoplasia, Fertility-sparing Surgery. Basic parameters: 18 years — 45 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
We will investigate the safety and efficiency of fertility-sapring treatment in ypung women witg endometrial cancer and endometrial intraepithelial hyperplasia
Detailed description
A multi-center prospective study on the oncological and reproductive outcomes and quality of life in young woman after fertility-sparing treatment of endometrial cancer and endometrial intraepithelial hyperplasia
Primary outcome measures
- Relaps of endometrial cancer or EIN after fertility-sparing treatment [Time frame: from enrollment to 2 years after fertility-sparing treatment]
Secondary outcome measures (1)
- Live birth rate in women that has been treated with fertility-sparing treatment for EC or EIN [Time frame: From start of study to 2 years after fertility-sparing treatment]
Eligibility criteria
Inclusion criteria
- Fertility sparing treatment of EC and EIN.
- 18-45 Years old
- From start study (Jan 2025 - end study Jan 2028)
- All centras in Sweden
Exclusion criteria
- Not English och Swedish speaking
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Case-only
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06745427 · 2024048701