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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT05260788
Other study ID # 21-5338
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date March 2022
Est. completion date March 2025

Study information

Verified date April 2022
Source University Health Network, Toronto
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date March 2025
Est. primary completion date March 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility 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. 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.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Cystoscopy
Standard of care cystoscopy procedure

Locations

Country Name City State
Canada Princess Margaret Cancer Centre Toronto Ontario

Sponsors (1)

Lead Sponsor Collaborator
University Health Network, Toronto

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Video recording of Cystoscopy 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. At study completion, up to 2 years
Primary Contouring of 3D bladder rendering To determine the feasibility of contouring the mucosal disease on the 3D bladder rendering. At study completion, up to 2 years
Primary Registering bladder shape To determine the feasibility of registering the bladder shape to a CT/MR scan of the patient using deformable shape methods. At study completion, up to 2 years
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