Prince of Wales Hospital
Hong Kong
Location contact
Chi Fai NG
SUB_INVESTIGATOR
Chi Hang YEE
SUB_INVESTIGATOR
Jeremy Yuen Chun TEOH, MBBS, FRCSEd
CONTACT
Ka Fung Peter CHIU
SUB_INVESTIGATOR
Qinyang LIU
SUB_INVESTIGATOR
Sui Yan LAU
CONTACT
NCT Number: NCT07095751
This is a single-arm study investigating the safety, feasibility and diagnostic performance of AI-assisted Uro-Cam catheter assessment that will be performed at the Prince of Wales Hospital. All patients who are referred to the urology outpatient clinic for hematuria workup, and bladder cancer patients who require follow-up cystoscopy, will be screened for study eligibility. If eligible, patients will be recruited into the study with a proper informed consent. All recruited patients will undergo the AI-assisted Uro-Cam catheter assessment followed by a conventional flexible cystoscopy. The study will be conducted in accordance with the Declaration of Helsinki, and it will be registered in ClinicalTrials.gov.
An AI-assisted Uro-Cam catheter assessment will be arranged for all recruited study subjects. After the AI-assisted Uro- Cam catheter assessment, a conventional flexible cystoscopy will be conducted in the same session. Biopsy will be taken from any suspicious lesion detected upon AI-assisted Uro-Cam catheter assessment or conventional flexible cystoscopy.
After all the procedures, an End-of-study visit will be arranged 4-6 weeks later. The primary outcomes include 30-day complications, and the technical success rate of the AI-assisted Uro-Cam catheter assessment. 30-day complications will be assessed and grading according to the Clavien-Dindo classification. Technical success is defined by the completion of the whole Uro-Cam catheter assessment. The secondary outcomes include the AUC, sensitivity, specificity, positive predictive value, and negative predictive value in detecting histologically confirmed bladder cancer.
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Not applicable
Hong Kong
Chi Fai NG
SUB_INVESTIGATOR
Chi Hang YEE
SUB_INVESTIGATOR
Jeremy Yuen Chun TEOH, MBBS, FRCSEd
CONTACT
Ka Fung Peter CHIU
SUB_INVESTIGATOR
Qinyang LIU
SUB_INVESTIGATOR
Sui Yan LAU
CONTACT
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
As stated in AI Uro-Cam arm description
Time frame: Thirty days after the allocated treatment
30-day complications will be assessed and grading according to the Clavien-Dindo classification.
Time frame: Immediately post-operative
Technical success is defined by the completion of the whole Uro-Cam catheter assessment.
Time frame: Thirty days after the allocated treatment
AUC, sensitivity, specificity, positive predictive value and negative predictive value in detecting bladder cancer will also be evaluated and recorded.
Contact information is provided by the study sponsor or research team.
Chinese University of Hong Kong
Other
Pilot Study on Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder Cancer
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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