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Clinical Trials in Canada / NCT03142802
Active, not recruiting Not applicable

Low-Dose CT - Stage I Testicular Cancer

NCT03142802 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2005-09-16
Last updated
2026-06-23

Condition(s) studied

Testicular Cancer

Investigational drug(s) / intervention(s)

Low-dose computed tomography (LDCT)

Low-dose computed tomography (LDCT): In phase A of the study, patients will undergo conventional CT along with low dose CT. If patients have a normal conventional CT and a satisfactory low dose CT, they will move onto Phase B of the study in which they will undergo surveillance using low-dose CT. Three outcomes are possible with low-dose CT surveillance: 1. Normal LDCT: \- Patient continues on the study (i.e. continued surveillance) 2. Suspicious LDCT: \- Will undergo conventional CT and if results are normal, patient will continue on study. If conventional CT is abnormal, they will be taken off study 3. Elevated serum tumour markers or other evidence of metastatic disease: * Patient goes off study

Study summary

Patients with primary germ cell cancer of the testicles confined to the testis can avoid adjuvant treatment by entering a surveillance protocol. In the surveillance protocol, patients are followed for up to ten years with serial computed tomography scans to detect recurrence. Multiple CT scans expose patients to a significant amount of radiation, which may be associated with an increased risk of secondary malignancies. This study hypothesizes that low dose CT scans are as effective as standard dose CT scans in detecting disease recurrence in this setting and will significantly reduce radiation exposure in this group of patients.

Eligibility

Sex
MALE
Min age
18 Years
Max age
100 Years
Healthy volunteers
No
Inclusion Criteria: * Phase A: * Newly diagnosed testicular germ cell testicular cancer (GCT) with no clinical or tumour marker evidence of metastases * Stage I disease according to UICC stage groupings and currently on surveillance (in Year 1 of non-seminoma surveillance or year 1 or 2 of seminoma surveillance) * ECOG performance status 0 or 1 * Phase B: * Stage I disease according to UICC stage Groupings * Initial Low dose CT considered by study radiologist to be of sufficient quality to allow surveillance using LDCT protocol Exclusion Criteria: * any medical conditions that render the patient ineligible to undergo the protocol or procedure

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University Health Network, Princess Margaret Hospital Toronto Ontario

More University Health Network, Toronto trials in Canada

Other trials for the same condition

Official registry record

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 NCT03142802 on ClinicalTrials.gov ↗ ← All trials in Canada