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Study identifier: NCT06749600 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Clinical Management and Outcomes of Primary Ovarian Leiomyosarcoma

Condition: Primary Ovarian Leiomyosarcoma  ·  Sponsor: Azienda USL Reggio Emilia - IRCCS

PhaseN/A
Planned participants30
Who can joinFemale, 18 Years to 99 Years
Healthy volunteersNo

About this study

This observational study aims to gather comprehensive data on primary ovarian leiomyosarcoma (POLMS). This extremely rare malignancy accounts for less than 3% of primary ovarian malignancies and has an incidence of only 1% among ovarian cancers. This national, retrospective and prospective multicenter study will collect and analyze historical cases of POLMS with remote diagnoses accessed through clinical case reviews and newly identified cases. The study aims to expand a previously identified series of 113 cases described in the literature, uncovering patterns in diagnosis, treatment, and outcomes and ultimately establishing evidence-based guidelines for the optimal management of this rare and aggressive cancer.

This description comes directly from the study's public registry record.

Talk to the study team

Vincenzo Dario Mandato, MD  ·  +39 0522 295467  ·  vincenzodario.mandato@ausl.re.it

Always discuss trial participation with your own doctor first.

Locations (10)

AOU Policlinico di ModenaModena, Italy, ItalyRecruiting
Azienda Ospedaliero Universitaria di Parma - S.C. Ostetricia e GinecologiaParma, PR, ItalyRecruiting
Azienda USL IRCCS di Reggio EmiliaReggio Emilia, RE, ItalyRecruiting
Malzoni - AvellinoAvellino, ItalyRecruiting
Azienda Ospedaliero Universitaria Policlinico "G.Rodolico - San Marco" - CataniaCatania, ItalyRecruiting
IRCCS Ospedale San RaffaeleMilan, ItalyRecruiting
Fondazione Irccs San Gerardo Dei TintoriMonza, ItalyRecruiting
IRCCS Istituto Nazionale Tumori Fondazione PascaleNaples, ItalyRecruiting
Università degli Studi di Napoli Federico IINaples, ItalyRecruiting
Ospedale "Sacro Cuore"Verona, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT06749600