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WEST-KOaST Study: WES Analysis of Testicular Cancer Patientsand Their First-degree Family Members (West-KOaSt)

S

San Donato Group (GSD)

Status

Not yet enrolling

Conditions

Testicular Cancer

Treatments

Genetic: Analysis of biological samples of saliva from testicular cancer patients and from their first-degree family members

Study type

Interventional

Funder types

Other

Identifiers

NCT06142500
West KOaSt

Details and patient eligibility

About

The project aims to identify the possible risk factors regarding the onset of the disease and to evaluate genes and gene modifications responsible for the onset od testicular cancer.

Full description

Testicular tumor represents a relatively rare disease that hit young-adults men. It represents 1% of all male cancers and 5% of all urological male tumors. Its incidence grow year by year. In the field of the oncological research, the lack of knowledge about genes related to this disease represent a very relevant clinical question. For this reason this project aims to collect biological samples of saliva from testicular cancer patients and from their first-degree family members; demographic-clinical variables will be also collected in order to draft a comprehensive panel of genes and gene modifications related to the testicular cancer, combining this survey with a very detailed description of this cohort of patient in terms of clinical features and quality of life.

Enrollment

4,500 estimated patients

Sex

All

Ages

18 to 90 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Male testicular cancer patients with an age > 18 and < 90
  • First degree family members of Male testicular cancer patients with an age > 18 and < 90
  • Ability to read and sign the informed consent
  • Diagnosis of testicular cancer for the experimental group

Exclusion criteria

  • Female for the experimental group
  • Second degree family members of Male testicular cancer patients
  • People with an age < 18 and > 90
  • Diagnosis different from testicular cancer for the experimental group Incapacity to read and sign the informed consent

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

4,500 participants in 2 patient groups

Patients with testicular cancer
Experimental group
Description:
Patient with testicular cancer
Treatment:
Genetic: Analysis of biological samples of saliva from testicular cancer patients and from their first-degree family members
First-degree family members of patients with testicular cancer
Active Comparator group
Description:
First-degree family members of patients with testicular cancer
Treatment:
Genetic: Analysis of biological samples of saliva from testicular cancer patients and from their first-degree family members

Trial contacts and locations

0

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Central trial contact

Andrea Salonia, MD; Alessia d'Arma, MSc

Data sourced from clinicaltrials.gov

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