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99mTc-CNDG Injection in the Diagnosis of Malignant Tumors

A Prospective Study to Explore the Performance and Efficacy of 99mTc-CNDG Injection in Malignant Tumors

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06030817
Enrollment
100
Registered
2023-09-11
Start date
2023-08-11
Completion date
2025-12-31
Last updated
2023-09-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Malignant Tumor

Brief summary

Currently, 18F-fluorodeoxyglucose (18F-FDG) is the most widely used tumor imaging agent in clinical practice. However, the production of 18F requires accelerators and is associated with relatively high diagnostic costs, which to some extent limits its widespread clinical application. In comparison to Positron Emission Tomography (PET), Single Photon Emission Computed Tomography (SPECT) devices are more abundant and offer lower diagnostic expenses. With the utilization of Cadmium Zinc Telluride (CZT) crystals in SPECT and advancements in image reconstruction techniques, the resolution and sensitivity of SPECT is continually improving. Therefore, the development of a simplified and cost-effective novel SPECT tumor imaging agent holds significant practical significance. This study involved the design and synthesis of a glucose-derived ligand with a linker containing seven methylene units and an isonitrile group (CN7DG). The CN7DG ligand was labeled with 99mTc to prepare a more lipophilic 99mTc-CN7DG complex, aiming to investigate a novel SPECT imaging agent for tumor imaging.

Interventions

DIAGNOSTIC_TEST99mTc-CNDG SPECT/CT

Explore the imaging characteristics of 99mTc-CNDG and its diagnostic efficacy in tumor patients.

Sponsors

Peking Union Medical College Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* 18-70 years old * Patients diagnosed with malignant glioma, colorectal cancer, pancreatic cancer, lung cancer, breast cancer, or other malignant tumors through imaging techniques such as MRI, CT, and ultrasound, and who are scheduled for surgical resection or biopsy * Solid tumor sizes greater than 2cm * Voluntarily agree to participate and sign an informed consent form * Can provide complete surgical records, pathological results, control data, and clinical follow-up results

Exclusion criteria

* Pre-treatment such as chemotherapy and targeted therapy has been administered * Pregnancy and breastfeeding * Claustrophobia * The condition is severe and difficult to cooperate with * Unable to obtain relevant control imaging data and clinical information

Design outcomes

Primary

MeasureTime frameDescription
Uptake value of 99mTc-CNDG in malignant tumorsthrough study completion, an average of 1 yearThe uptake value was measured in the malignant lesions on 99mTc-CNDG SPECT/CT.
Lesions detected by 99mTc-CNDG SPECT/CTthrough study completion, an average of 1 yearThe number of target lesions was calculated by 99mTc-CNDG SPECT/CT
Compared with 18F-FDG PET/CT or CECTthrough study completion, an average of 1 yearThe number of lesions detected by 99mTc-CNDG SPECT/CT was compared with 18F-FDG PET/CT or CECT

Countries

China

Contacts

Primary ContactHongli Jing
annsmile1976@sina.com+86-18600586399

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026