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Clinical Trials in China / NCT07794813
Recruiting Observational

Trop2-targeting NIR-II Molecular Probe for Precision Diagnosis of Oral Cancer

NCT07794813 · tracked via the Priya Life Science China tracker
Sponsor
Yunnan Cancer Hospital
Phase
Observational
Started
2024-12-03
Last updated
2026-08-31

Condition(s) studied

Oral Squamous Cell Carcinoma (OSCC)Diagnosis

Investigational drug(s) / intervention(s)

TTP-ICG incubation solution

TTP-ICG incubation solution: Fresh clinical specimens will be incubated with TTP-ICG with different concentrations and times.

Study summary

Given the morphological and clinical similarities between certain oral malignant neoplasms and benign conditions such as oral ulcerations or inflammatory lesions, the potential for misdiagnosis is significant. Currently, histopathological examination via tissue biopsy remains the diagnostic gold standard; however, this approach is inherently invasive and may yield incomplete diagnostic results due to sampling limitations and spatial heterogeneity of the lesion. These challenges underscore the urgent need for the development of simple, non-invasive, cost-effective, and real-time in vivo imaging modalities. To address this, the investigators propose the utilization of a previously developed near-infrared II (NIR-II) fluorescent molecular imaging probe, TTP-ICG, which exhibits high specificity for TROP2, a transmembrane glycoprotein frequently overexpressed in oral squamous cell carcinoma (OSCC). This study will evaluate the diagnostic accuracy of OSCC through localized application of the TROP2-targeted probe via clinical specimens being soaked in TTP-ICG solution. Furthermore, the investigators aim to explore the feasibility of employing a mouth wash-based delivery system for the probe, with the ultimate goal of establishing a precise, minimally invasive, and cost-effective real-time imaging strategy for the early detection and diagnosis of OSCC. Such an approach has the potential to significantly enhance diagnostic precision, improve patient outcomes, and increase survival rates.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Age range: 18-75 years old; * Patients with oral cancer or benign oral tumors who plan to undergo surgical intervention; * Preoperative coagulation function test was normal; ④ No serious underlying diseases; ⑤ WHO Physical Status Score 0-2 points; * Sign the informed consent form; Exclusion Criteria: * Suffering from other invasive malignant tumors; * Surgery cannot be performed for other serious illnesses; ③ Suffering from mental disorders and unable to sign informed consent forms on their own; * The subject requests to withdraw from the clinical trial; ⑤ The researchers believe that it is not appropriate for them to continue participating in this clinical trial.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Yunnan Cancer Hospital Kunming Yunnan Recruiting

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07794813 on ClinicalTrials.gov ↗ ← All trials in China