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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05140083
Other study ID # FirstAHFujian13
Secondary ID
Status Recruiting
Phase Phase 1
First received
Last updated
Start date April 25, 2021
Est. completion date December 30, 2024

Study information

Verified date September 2023
Source First Affiliated Hospital of Fujian Medical University
Contact Weibing Miao, MD
Phone 86-0591-87981618
Email miaoweibing@126.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To evaluate the potential usefulness of 68Ga-NOTA Evans Blue (68Ga-NEB) positron emission tomography/computed tomography (PET/CT) for the diagnosis of primary and efficacy assessment in lymphatic system related diseases.


Description:

Subjects with lymphatic system related diseases underwent 68Ga-NEB PET/CT either for a primary diagnosis or for efficacy assessment. Anomalies were detected by visual analysis and quantitative analysis of maximum standard uptake value (SUVmax). To compare the diagnostic sensitivity of 68Ga-NEB PET/CT lymphatic imaging with other lymphatic imaging such as 99mTc-dextran for lymphatic system related diseases.


Recruitment information / eligibility

Status Recruiting
Enrollment 80
Est. completion date December 30, 2024
Est. primary completion date December 30, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - adult population (aged between18 years and 80 years) - patients with suspected or new diagnosed or previously treated lymphatic system related diseases - patients who had scheduled 68Ga-NEB PET/CT scan - patients who were able to provide informed consent (signed by participant, parent or legal representative) and assent according to the guidelines of the Clinical Research Ethics Committee Exclusion Criteria: - patients with pregnancy - the inability or unwillingness of the research participant, parent or legal representative to provide written informed consent.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
68Ga-NOTA Evans Blue
Each subject receives a single subcutaneous injection of 68Ga-NOTA Evans Blue, and undergo PET/CT imaging within the specific time.

Locations

Country Name City State
China Department of Nuclear Medicine, First Affiliated Hospital of Fujian Medical University Fuzhou Fujian

Sponsors (1)

Lead Sponsor Collaborator
First Affiliated Hospital of Fujian Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visual analysis of lymphatic patency The bilateral lymphatic description on 68Ga-NEB PET/CT and lymphatic SPECT imaging were compared. The patency of lymphatic vessels (including lymphatic disruption, dermal distribution, and so on, results are indicated by 0 and 1) are shown in two imagings were recorded respectively. through study completion, an average of 3 years
Primary Standardized uptake value (SUV) Standardized uptake value (SUV) of 68Ga-NEB for each target lesion of subject. through study completion, an average of 3 years
Secondary Diagnostic efficacy The sensitivity of 68Ga-NEB PET/CT and lymphatic SPECT imaging were calculated. through study completion, an average of 3 years
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