Skip to main content
Clinical Trials/NCT06030817
NCT06030817
Recruiting
Not Applicable

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

Peking Union Medical College Hospital1 site in 1 country100 target enrollmentAugust 11, 2023
ConditionsMalignant Tumor

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Malignant Tumor
Sponsor
Peking Union Medical College Hospital
Enrollment
100
Locations
1
Primary Endpoint
Compared with 18F-FDG PET/CT or CECT
Status
Recruiting
Last Updated
2 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
August 11, 2023
End Date
December 31, 2025
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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

Outcomes

Primary Outcomes

Compared with 18F-FDG PET/CT or CECT

Time Frame: through study completion, an average of 1 year

The number of lesions detected by 99mTc-CNDG SPECT/CT was compared with 18F-FDG PET/CT or CECT

Lesions detected by 99mTc-CNDG SPECT/CT

Time Frame: through study completion, an average of 1 year

The number of target lesions was calculated by 99mTc-CNDG SPECT/CT

Uptake value of 99mTc-CNDG in malignant tumors

Time Frame: through study completion, an average of 1 year

The uptake value was measured in the malignant lesions on 99mTc-CNDG SPECT/CT.

Study Sites (1)

Loading locations...

Similar Trials