Study on the Quality of Life and Functional/Oncological Outcome of Testicular Cancer Patients
Condition(s) studied
Investigational drug(s) / intervention(s)
Observation of testicular cancer patients: Collection of clinical data of all patients suffering from neoplastic testicular pathology undergoing surgery
Study summary
The research aims to collect data in order to report the main problems related to the testicular cancer; To reach this aim, this study proposes to create a database of the testicular cancer condition.
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.
Eligibility
Primary outcome measure(s)
- Clinical data — Baseline
Collection of clinical data - Adjuvant therapy — Baseline
Which type of adjuvant therapy carried out (chemotherapy - radiotherapy - retroperitoneal lymphadenectomy) - lactate dehydrogenase — Follow up after 6 months from baseline
Oncological follow-up through enzymatic value - Testicular objective examination — Baseline
Number and size (via Prader orchidometer) of the testicles - Testicular objective examination - cysts — Baseline
Evaluation presence of cysts - Testicular objective examination - nodules — Baseline
Evaluation presence of nodules - Testicular objective examination - varicocele — Baseline
Evaluation presence of varicocele - Testicular objective examination - hydrocele — Baseline
Evaluation presence of hydrocele - α-feto protein — Follow up after 6 months from baseline
Oncological follow-up through enzymatic value - β human Chorionic Gonadotropin — Follow up after 6 months from baseline
Oncological follow-up through hormonal value - carcinoembryonic antigen — Follow up after 6 months from baseline
Oncological follow-up through hormonal value
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| IRCCS Ospedale San Raffaele | Milan | Lombardy | Recruiting |
More IRCCS San Raffaele trials in Italy
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06389409 on ClinicalTrials.gov ↗ ← All trials in Italy