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NCT Number: NCT05733806

Study on Gynecological Rare Cancers

This is a prospective, observational, multicenter study on gynecological rare tumors.

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Key information

Conditions

Gynecologic Cancer

Sex eligibility

Female

Study type

Observational

Primary location

Ginecologia e Ostetricia, IRCCS Ospedale San Raffaele, Milan, Italy

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About this study

This is a prospective registry aimed to better understand prognosis, clinical and pathological features, management of this rare cancer conditions for improving standard of care.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • rare gynecological malignancies
  • written informed consent
  • patient fit for follow-up

Exclusion criteria

-written informed consent not provided

Treatment and study plan

chemotherapy, surgery

Other

this is an observational prospective study, therefore no intervention is planned. Patients perform medical and surgical treatment as per standard of case.

Primary outcomes

  1. Prevalence of gynecologic rare malignancies

    Time frame: 5 years

    To describe the prevalence of gynecologic rare tumors

Interested in participating?

Recruiting

Interested in participating?

Request Info

Sponsors and collaborators

Lead sponsor

National Cancer Institute, Naples

Other

Registry information

Official study title

Prospective, Multicenter, Observational Study on Rare Gynecological Cancers

Acronym: MITO9B

Important dates

Study start
2019
Primary completion
2025
Study completion
2030
First posted
Feb 17, 2023
Registry last updated
Feb 23, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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