Interest of Magnetic Resonance Imaging in the Diagnosis of Upper Urinary Tract Invasive Tumours

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity Hospital, Toulouse

About this trial

Upper urinary tract invasive cancer magnetic resonance imaging diagnosis

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patient over 18 years of age with a suspected upper urinary tract tumour based on the presence of a suspicious lesion on a uro-computed tomography scan

Have given free, informed and signed consent

Be affiliated to a social security scheme

Disqualifiers

Renal failure not allowing the injection of iodinated contrast media (Glomerular filtration rate <30mL/min)

Subject under legal protection (guardianship or curatorship)

Pregnant or breastfeeding woman

Person participating in another research study or having participated in a protocol with an exclusion period still in progress at inclusion

Trial design

Design model

Single group

Treatments tested in this trial

  • Upper urinary tract magnetic resonance imaging

    Radiation

    Patients with a suspected malignant tumour of the upper urinary excretory tract based on the presence of a suspicious lesion on a uro-computed tomography scan will have a diagnostic magnetic resonance imaging of the urinary tract with Gadolinium-based contrast agents

Treatment groups

178 Participants
are divided into 1 treatment group
Group A: Patients with upper urinary tract tumourExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Diagnostic validity (composite criteria sensitivity and specifcity) of a predefined magnetic resonance imaging sequence in the diagnosis of upper urinary tract invasive tumour

Diagnostic validity (sensitivity and specifcity) of a predefined magnetic resonance imaging sequence in the diagnosis of upper urinary tract invasive tumour (taking as reference the pathological analysis \[gold standard\] or biopsy with 3 months Uro-CT).

Time frame
3 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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