MedPath

Mapping 3D Bladder

Withdrawn
Conditions
Bladder Cancer
Registration Number
NCT05260788
Lead Sponsor
University Health Network, Toronto
Brief Summary

This is a single centre, single arm feasibility study assessing the feasibility of using computer vision methods to recreate the 3D bladder shape and to then map the cystoscopy images onto this bladder shape. If feasible, this 3D reconstructed shape would be spatially registered to radiological images (CT, MR) that are then used during radiation treatment planning. This analysis would not be used for making any clinical treatment decisions on the patient.

Detailed Description

Not available

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • 18 years of age or older.
  • Clinical suspicion or histologic diagnosis of bladder tumour suitable for endoscopic evaluation.
  • Intention to treat using external beam radiation therapy as part of standard of care.
  • Ability to provide written informed consent to participate in the study.
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Exclusion Criteria
  • Prior complete or partial radiation therapy to bladder.
  • Contraindications to radiation therapy as determined by the treating physician.
  • Concurrent illness or condition that precludes subject from undergoing endoscopy or CT scanning.
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Video recording of CystoscopyAt study completion, up to 2 years

To determine the feasibility of using bladder endoscopic video images to reconstruct the three-dimensional shape of the bladder based on computer visions methods that employ feature extraction and triangulation and to map the endoscopy images onto the recreated 3D surface.

Contouring of 3D bladder renderingAt study completion, up to 2 years

To determine the feasibility of contouring the mucosal disease on the 3D bladder rendering.

Registering bladder shapeAt study completion, up to 2 years

To determine the feasibility of registering the bladder shape to a CT/MR scan of the patient using deformable shape methods.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Princess Margaret Cancer Centre

🇨🇦

Toronto, Ontario, Canada

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