99mTc-CNDG SPECT/CT in Brain Tumors

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorPeking Union Medical College Hospital

About this trial

The goal of this clinical trial is to evaluate the value of 99mTc-CNDG for diagnosis of brain tumors by comparing it with 18F-FDG-PET. The main questions it aims to answer are:

1. What is the diagnostic consistency between 99mTc-CNDG and 18F-FDG? 2. What is the correlation between the SUVmax value of 99mTc-CNDG and tumor type?

Participants will:

Receive18F-FDG-PET and 99mTc-CNDG examination within 2 weeks before surgery. Obtain pathological diagnosis by surgery or biopsy as the gold standard.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with clinical diagnosis of brain tumor;

Be at least 18 years old;

The final pathological results could be obtained by surgery or biopsy;

Informed consent and the ability to be followed up;

Disqualifiers

Insulin-dependent diabetes mellitus or fasting blood glucose >7 mmol/L before 99mTc-CNDG injection;

Severe liver or kidney disease (serum creatinine level >3.0mg/dL or any liver enzyme level ≥ 5 times the upper limit of normal);

Severe hypersensitivity or hypersensitivity to radiocontrast agents;

Claustrophobia (inability to undergo SPECT/CT or PET/CT scans);

Trial design

Design model

Single group

Treatments tested in this trial

  • 99mTc-CNDG SPECT/CT

    Diagnostic test

    FDG-PET and 99mTc-CNDG will be performed within 2 weeks before surgery.

Treatment groups

30 Participants
are divided into 1 treatment group
Group A: intracranial tumorExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

SUVmax

1\. Diagnostic consistency evaluation of 99mTc-CNDG and 18F-FDG; 2.Correlation of SUV value of 99mTc-CNDGwith tumor type

Time frame
1month

Secondary outcomes

Other outcomes

Sponsors and contacts

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