a SIngle Center Study of Post-operative STEReotactic RAdiotherapY for Endometrial Cancer

Recruiting N/A Interventional Study
Endometrial Cancer
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 80
Sex
Female
Study type
Interventional
Purpose
Treatment
Participants needed
60 (estimated)
Sponsor
ARNAS Civico Di Cristina Benfratelli Hospital · Other
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About This Trial

The primary endpoint of the present prospective study is to assess the outcomes in terms of acute toxicity of post-operative stereotactic radiotherapy for endometrial cancer

Trial Locations
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Eligibility Criteria
* Age 18-80 years * ECOG PS ≤ 2 or KPS ≥ 70% * Patients diagnosed with endometrial cancer (endometrioid, serous cell, clear cell, carcinosarcoma) FIGO stage IB-IIIC1 candidate to post-operative external beam radiotherapy, based on molecular and histological findings * Indications for chemotherapy an…
Contacts

FRANCESCO CUCCIA, MD

+393334393336

francesco.cuccia@arnascivico.it

CONTACT

GIUSEPPE FERRERA, MD

+393471533715

giuseppe.ferrera@arnascivico.it

CONTACT