Study on the Quality of Life and Functional/Oncological Outcome of Testicular Cancer Patients
NCT ID: NCT06389409
Last Updated: 2024-04-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
3000 participants
OBSERVATIONAL
2010-08-24
2040-08-31
Brief Summary
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From this perspective, the aim of this project is the improving of scientific knowledge of the disease and develop appropriate and effective procedures for the diagnosis and treatment of the patient.
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Detailed Description
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From these general epidemiological coordinates it can be deduced that this pathology could affects a young segment of the population; It must be underlined that a pathology is peculiar due to the impact it has on the affected individual, who must be treated not only from an oncological point of view but also with regards to the sexual, reproductive and psychological-relational aspects. Such complexity requires a systematic and detailed approach to examine all aspects.
The creation of this database let to have a follow up above all an extension over time that is not present in the literature, especially towards the functional aspects of this condition.
The database will represent a resource for future research.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Patient with testicular cancer
* subjects suffering from suspected neoplastic testicular pathology candidates for testicle removal surgery
* patients suffering from neoplastic testicular pathology requiring removal of the retroperitoneal lymph nodes
Observation of testicular cancer patients
Collection of clinical data of all patients suffering from neoplastic testicular pathology undergoing surgery
Interventions
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Observation of testicular cancer patients
Collection of clinical data of all patients suffering from neoplastic testicular pathology undergoing surgery
Eligibility Criteria
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Inclusion Criteria
* patients suffering from neoplastic testicular pathology requiring removal of the retroperitoneal lymph nodes
* subjects \> 18 years old
* subjects with at least elementary education
* signature of informed consent
Exclusion Criteria
* presence of mental or physical disability that may prevent the patient from satisfying the requirements of the protocol
18 Years
MALE
No
Sponsors
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IRCCS San Raffaele
OTHER
Responsible Party
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Andrea Salonia
Professor
Principal Investigators
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Andrea Salonia, MD
Role: PRINCIPAL_INVESTIGATOR
IRCCS Ospedale San Raffaele
Locations
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IRCCS Ospedale San Raffaele
Milan, Lombardy, Italy
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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Protocollo N.2009 Testicolo
Identifier Type: -
Identifier Source: org_study_id
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