Recruiting

Trop2-targeting NIR-II Probe for Non-Muscle-Invasive Bladder Cancer

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What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Urogenital Diseases+12

+ Non-Muscle Invasive Bladder Neoplasms

+ Urinary Bladder Diseases

From 18 to 80 Years
+7 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Case-Only

Examining characteristics of individuals with a disease in order to identify genetic or environmental factors contributing to the condition.
Observational
Study Start: January 2025
See protocol details

Summary

Principal SponsorYunnan Cancer Hospital
Study ContactShengjie Lin, Doctor of MedicineMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: January 17, 2025

Actual date on which the first participant was enrolled.

This study is designed to improve the way non-muscle-invasive bladder cancer is identified during surgery. It focuses on using a special fluorescent probe called TTP-ICG to help doctors distinguish between cancerous and nearby non-cancerous tissues. This is important because accurately identifying cancerous tissue can lead to more effective surgeries and better outcomes for patients. By enhancing the precision of cancer detection, this study aims to address the current challenge of differentiating cancerous tissues, which can sometimes be difficult with traditional methods. Participants in the study undergo surgical treatment for bladder cancer. After surgery, the removed tissues are treated with a TTP-ICG solution and then analyzed. The tissues are soaked in the solution for a short time, after which they are rinsed and dried. A special imaging system captures images of the tissues, allowing researchers to measure fluorescent signals that help determine if the tissue is cancerous. The study evaluates the intensity of these signals to see how well the probe can differentiate between cancerous and non-cancerous tissues. This process includes detailed analysis to ensure accurate results, potentially offering a new way to enhance cancer surgery precision.

Official TitleTrop2-targeting the Second Near-Infrared Fluorescence(NIR-II ) Molecular Probe for Guided Identification of Non-Muscle-Invasive Bladder Cancer
NCT06972771
Principal SponsorYunnan Cancer Hospital
Study ContactShengjie Lin, Doctor of MedicineMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

30 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Case-only

These studies focus only on individuals who have a specific disease. Researchers examine patterns—often genetic or environmental—to uncover what might be linked to the condition.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 80 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Urogenital DiseasesNon-Muscle Invasive Bladder NeoplasmsUrinary Bladder DiseasesUrinary Bladder NeoplasmsCarcinomaFemale Urogenital Diseases and Pregnancy ComplicationsNeoplasmsNeoplasms by Histologic TypeNeoplasms by SiteNeoplasms, Glandular and EpithelialUrogenital NeoplasmsUrologic DiseasesUrologic NeoplasmsFemale Urogenital DiseasesMale Urogenital Diseases

Criteria

4 inclusion criteria required to participate
Adult patients between 18-80 years of age

Patients with suspected non-muscle-invasive bladder cancer scheduled to undergo surgical intervention.

Good operative candidate

Subject capable of giving informed consent and participating in the process of consent

3 exclusion criteria prevent from participating
Patients unable to participate in the consent process

Patients had contraindications to surgery, such as serious cardiopulmonary disease, coagulation dysfunction, etc

Other conditions that the researcher considers inappropriate to participate in the study

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Recruiting

Yunnan Cancer Hospital

Kunming, ChinaOpen Yunnan Cancer Hospital in Google Maps
Recruiting
One Study Center