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Recruiting Observational

Study on the Quality of Life and Pathological State in Patients Who Underwent Radical Cystectomy

NCT06170177 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2013-02-04
Last updated
2023-12-14

Condition(s) studied

Muscle-Invasive Bladder CarcinomaMuscle Invasive Bladder Urothelial CarcinomaBladder Cancer TNM StagingBladder Cancer Stage IIaBladder Cancer Stage IIbBladder Cancer Stage IVBladder LeiomyosarcomaBladder CancerBladder Cancer Stage IIBladder Cancer Stage IIIaBladder Cancer Stage IIIbBladder Cancer Stage IIIcBladder Urothelial CarcinomaProgression, DiseaseUrinary DiversionNeobladderRadical Cystectomy

Investigational drug(s) / intervention(s)

Radical Cystectomy

Radical Cystectomy: A radical cystectomy is an operation to remove the whole bladder

Study summary

Observational study on the quality of life and pathological state of patients underwent radical cystectomy.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * subjects underwent radical cystectomy * \> 18 years old * Ability to read and sign the informed consent Exclusion Criteria: * Age \<18 years * Inability to read and sign the informed consent

Primary outcome measure(s)

  • obtain health benefit for the patients themselves and for future patients underwent radical cystectomy — Baseline and Follow-up. 1 Annual follow-up until the patient decides to stop providing follow-up responses or until the date of death from any cause.
    All patients, before underwent radical cystectomy, receive a diary in which we ask a detailed clinical history of the patient with their symptoms, diagnosis and previous urological e non urological treatments performed before the operation. A detailed intraoperative, postoperative and follow-up clinical history.
  • improve the patient's scientific knowledge and develop new procedures for the diagnosis and treatment of the patient — Baseline and Follow-up. 1 Annual follow-up until the patient decides to stop providing follow-up responses or until the date of death from any cause.
    Through the collection of a detailed clinical history of the patient in which themselves report symptoms, diagnosis and previous urological and non-urological treatments and also through the medical record.

Trial sites (1)

FacilityCityRegionStatus
IRCCS Ospedale San Raffaele Milan MI Recruiting
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 NCT06170177 on ClinicalTrials.gov ↗ ← All trials in Italy