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

No phase Interventional Testicular Cancer

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Analysis of biological samples of saliva from testicular cancer patients and from their first-degree family members.
Who it may be relevant to
Registry conditions: Testicular Cancer. Basic parameters: 18 years — 90 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

WEST-KOaST Study: WES (Whole Exome Sequencing) Analysis of Testicular Cancer Patientsand Their First-degree Family Members

Overview

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.

Detailed 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.

Interventions

  • Genetic Analysis of biological samples of saliva from testicular cancer patients and from their first-degree family members
    The 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 descprition of this cohort of patient in terms of clinical features and quality of life

Primary outcome measures

  • Saliva biological sample [Time frame: Baseline]
Secondary outcome measures (1)
  • Demographic-clinical variables [Time frame: Baseline]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Non-randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Diagnostic

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06142500 · West KOaSt

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗