Observational study on rare gynecological cancers
Official title: Prospective, Multicenter, Observational Study on Rare Gynecological Cancers
Run by National Cancer Institute, Naples · NCT05733806 · Data updated 2026-11-12
This study is trying to learn more about rare gynecological cancers to improve treatment and care for patients facing these conditions.
Quick facts
| Study type | Observational |
|---|---|
| Sex | Women only |
| Enrollment | 500 (estimated) |
| Sponsor | National Cancer Institute, Naples Academic / other |
| Locations | 2 sites (Milan and 1 other locations) |
| Status | Recruiting |
| Started | October 14, 2019 |
| Main results expected | January 1, 2025 |
| Study ends | February 1, 2030 |
| Registry record updated | February 23, 2023 |
| Trial ID | NCT05733806 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are patients diagnosed with rare gynecological malignancies who can provide written informed consent and are fit for follow-up.
✕Probably not a fit
Patients who do not have rare gynecological cancers or cannot provide informed consent may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a prospective, observational, multicenter registry focused on understanding the prognosis, clinical and pathological features, and management of rare gynecological tumors. The study aims to gather comprehensive data to improve the standard of care for patients with these rare malignancies. Participants will be monitored over time to assess treatment outcomes and disease progression.
Why it matters
Potential benefit: If successful, this study could enhance the understanding and management of rare gynecological cancers, leading to improved patient outcomes.
How similar studies have gone: While there have been studies on gynecological cancers, this specific focus on rare malignancies is relatively novel and may provide new insights.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * rare gynecological malignancies * written informed consent * patient fit for follow-up Exclusion criteria -written informed consent not provided
Where it's running
-
Ginecologia e Ostetricia, IRCCS Ospedale San Raffaele
Milan, Italy Recruiting -
IRCCS Fondazione G Pascale
Naples, Italy Recruiting
Study contacts
- Principal investigator: Francesco Perrone, MD — IRCCS Fondazione G Pascale, Naples
- Study coordinator: Francesco Perrone, MD
- Email: f.perrone@istitutotumori.na.it
- Phone: 0039 081 1777 0276
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.