Actively Recruiting

Age: 18Years +
All Genders
ID06167356

Observational Study on the Occurrence of Possible Relapses and on the Quality of Life in Patients Who Underwent Endoscopic Resection Surgery for Bladder Cancer (TURBK).

Led by IRCCS San Raffaele · Updated on 2023-12-12

20000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are collecting and studying data on adult patients who have undergone specific endoscopic resection surgeries for non-muscle invasive bladder cancer, including TURBK, MAPPING, TURBK SECOND LOOK, and BLADDER BIOPSIES. The aim is to observe the occurrence of possible relapses and assess the quality of life in these patients over time. Patients will be followed for about 10 years starting from their surgery date. Follow-up will be done yearly through the patient's preferred contact method, such as phone, email, or home visits, by the Urology Department staff. Data collected will cover pre-hospitalization symptoms and clinical details, hospitalization information, and annual quality of life questionnaires. Throughout the study, patient information will be securely stored in a database following strict privacy and good clinical practice standards. The researchers will measure health benefits for current and future patients and aim to improve scientific knowledge and develop new diagnostic and treatment procedures. Patients may stop providing follow-up responses at any time, and data collection will continue until then or until death.

CONDITIONS

Brief Title

Study on the Occurrence of Possible Relapses and on the Quality of Life in Patients Who Underwent TURBK.

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years or older
  • Patients with non-muscle invasive bladder cancer
  • Indication to cancer removal through endoscopic resection surgery
  • Ability to read and sign the informed consent
Not Eligible

You will not qualify if you...

  • Age under 18 years
  • Inability to read and sign the informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Surgery and Immediate Post-operative Care

Duration - Hospitalization period

Participants undergo endoscopic resection surgery for bladder cancer and related hospitalization.

Long-term Monitoring

Duration - Approximately 10 years

Participants are followed for approximately 10 years after surgery with annual quality of life questionnaires and follow-up contacts by phone, email, or mail.

Annual follow-up contacts

Trial Site Locations

Total: 1 location

1

IRCCS Ospedale San Raffaele

Milan, MI, Italy, 20132

Actively Recruiting

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Research Team

F

Francesco Montorsi, MD

G

Giusy Burgio, MSc

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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