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Targeted Translocator Protein PET Imaging Evaluate Neuroinflammation of the Chronic Pain Patients

Targeted Translocator Protein PET Imaging Evaluate Neuroinflammation of the Chronic Pain Patients

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06701734
Enrollment
60
Registered
2024-11-22
Start date
2024-12-01
Completion date
2028-12-31
Last updated
2024-11-22

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

Conditions

Chroinc Pain, Microglial Activation, PET

Brief summary

Chronic pain is a major public health issue, which seriously affects patients' quality of life. Neuroinflammation is an important mechanism resulting in chronic pain. Translocator protein (TSPO) has served as a marker of microglial activation and neuroinflammation. 18F-DPA714, a tracer targeted TSPO, can be used to evaluate the microglial activation and neuroinflammation in vivo by PET imaging.Recent and increasing studies have found changes in TSPO and its ligands in various chronic pain models. Reversing their expressions has been shown to alleviate chronic pain in these models, illustrating the effects of TSPO and its ligands.The investigators aim to explore the clinical feasibility used 18F-DPA714 PET imaging to monitor microglial cells activation of center nervous system in chronic pain patients. This study might reveal significant neuroinflammatory process in the center nervous system of the chronic pain patients. The results of this study might provide a new biomarker of disease pathological progression and indicates that TSPO-based therapy may become an alternative strategy for treating chronic pain.

Interventions

None listed

Sponsors

Weibing Miao, PhD
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* chronic pain patients * Written informed consent was provided by the patients and their family

Exclusion criteria

* history of head trauma , epilepsy, claustrophobia, rheumatic or autoimmune diseases, psychiatric disorders, severe somatic diseases (neurological,cardiovascular, etc.),previous heart or brain surgery, substance abuse, inability to refrain from hypnotics, magnetic implants, pregnancy, lactation

Design outcomes

Primary

MeasureTime frameDescription
Standardized Uptake Value2 yearsMeasures of specific binding of 18F-DPA-714 measures of specific binding of the tracer

Contacts

Primary ContactQianqian Xue
xueqian124@163.com+8618558799064

Outcome results

None listed

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