ClinicalTrials.gg
Not yet recruitingNCT06745427PreFerEC/EINUpdated Dec 20, 2024

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

An observational study in Endometrial Cancer, Endometrial Intraepithelial Neoplasia and Fertility-sparing Surgery, sponsored by Region Stockholm. Not yet recruiting. Open to female participants aged 18 Years to 45 Years. Per ClinicalTrials.gov, last updated 2024-12-20.

Sponsored by Region Stockholm · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
100
Ages
18 Years to 45 Years
Sex
Female
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Study summary

We will investigate the safety and efficiency of fertility-sapring treatment in ypung women witg endometrial cancer and endometrial intraepithelial hyperplasia

Read the 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

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Conditions studied

  • Endometrial Cancer
  • Endometrial Intraepithelial Neoplasia
  • Fertility-sparing Surgery
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In context

Endometrial Neoplasms

1,425 studies on the registry are indexed under Endometrial Neoplasms; 473 are open to participants now.

This study's planned enrollment of 100 is below the median of 179 across 331 observational studies indexed under Endometrial Neoplasms.

Browse Endometrial Neoplasms studies →

Lead sponsor

Region Stockholm is the lead sponsor of 121 studies on the registry; 69 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All women in Sweden

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

Exclusion Criteria:

  • Not English och Swedish speaking
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Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
100 participants (estimated)
Patient registry
No
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What researchers measure

Primary outcomes

  1. Relaps of endometrial cancer or EIN after fertility-sparing treatment

    Relaps of endometrial cancer or EIN after fertility-sparing treatment

    Time frame: from enrollment to 2 years after fertility-sparing treatment

Secondary outcomes

  1. Live birth rate in women that has been treated with fertility-sparing treatment for EC or EIN

    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

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

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Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Jan 2025; primary completion for Jan 2028, 36 months later.

Of 130 non-industry observational studies under Endometrial Neoplasms, half reached primary completion within 105 months of starting (the median), counting those still running; a quarter within 32 and three quarters within 206. This study's planned 36 months is below that.

Counting every sponsor, half of 150 studies reached it within 105 months; a quarter within 32 and three quarters within 207.

How these figures are worked out, and which studies are left out of them.

Registered
Dec 17, 2024
First posted
Dec 20, 2024
StartEst.
Jan 15, 2025
Primary completionEst.
Jan 15, 2028
CompletionEst.
Jan 15, 2030
Last update
Dec 20, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Dec 20, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06745427
Lead sponsor
Region Stockholm
Responsible party
Charlotta Riese (MD, Region Stockholm) — Principal investigator
First posted
Dec 20, 2024
Start date
Jan 15, 2025 (estimated)
Primary completion
Jan 15, 2028 (estimated)
Completion
Jan 15, 2030 (estimated)
Last update
Dec 20, 2024

Study contacts

Charlotta CR Riese, MD, PHD-student
Contact
charlotta.riese@ki.se
+46703440206
Kenny Rodriguez Wallberg, Proffessor
Contact
kenny.rodriguez-wallberg@ki.se
+46 73546 10 71

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Dec 2024. You cannot join it, but the record below documents what was studied.

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Discussion

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