Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06679920

Study With a Newly Optical Coherence Tomography Probe for Optimizing Bladder Cancer Diagnosis and Treatment

Led by Amsterdam UMC · Updated on 2024-12-06

15

Participants Needed

2

Research Sites

17 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to see if a new designed optical coherence tomography catheter can be used in bladder cancer in patients undergoing a transurethral resection of a bladder tumour. The main question it aims to answer is: \- Is the optical coherence tomography catheter feasible in capturing images of bladder tumours and normal bladder wall during a transurethral resection of a bladder tumour? Participants will undergo measurements with a new optical coherence tomography device during the transurethral resection of their bladder tumour(s).

CONDITIONS

Official Title

Study With a Newly Optical Coherence Tomography Probe for Optimizing Bladder Cancer Diagnosis and Treatment

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age > 18 years.
  • Have at least 1 suspected bladder tumour seen at cystoscopy.
  • Have a bladder that is accessible for cystoscopy.
  • Be in a physical condition to undergo a TURBT.
  • Provide written informed consent before any study procedures.
Not Eligible

You will not qualify if you...

  • Pregnant or lactating women.
  • Tumour only located at the bladder neck.
  • Tumour larger than 2 centimetres in diameter.
  • More than 5 tumours present.
  • Only a suspected flat lesion present.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Amsterdam University Medical Center

Amsterdam, North Holland, Netherlands, 1081HV

Not Yet Recruiting

2

Amsterdam University Medical Center

Amsterdam, Netherlands, 1081HV

Actively Recruiting

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Research Team

M

Marinka Remmelink, MD

CONTACT

J

Jorg R Oddens, MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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