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An Efficient Method for the Synthesis of [¹8F]FDOPA and Its Applications in Neurological and Oncologic PET Imaging

An Efficient Method for the Synthesis of [¹8F]FDOPA and Its Applications in Neurological and Oncologic PET Imaging

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500114524
Enrollment
Unknown
Registered
2025-12-15
Start date
2025-12-15
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Various neuroendocrine tumors, gliomas, and Parkinson’s disease

Interventions

Gold Standard:For tumor patients: pathological confirmation
For Parkinson’s disease: diagnosis based on the 2015 International Parkinson and Movement Disorder Society (MDS-PD) clinical diagnostic criteria.
Index test:[18F]FDOPA PET/CT imaging

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Voluntarily participates in this clinical study and signs a written informed consent form prior to any study-related procedures. (2) Has an expected survival of more than 3 months. (3) Patients with pathologically confirmed or clinically highly suspected pheochromocytoma/paraganglioma, neuroblastoma, glioma, gastrointestinal carcinoid tumor, medullary thyroid carcinoma, or clinically diagnosed Parkinson’s disease. (4) Newly diagnosed patients, or those who have completed prior antitumor therapy at least =1 month before enrollment. (5) Women and men of childbearing potential must agree to use strict and effective contraception after signing the informed consent, throughout the study period, and for 6 months after study completion. During the same period, male participants must refrain from donating sperm and female participants must not undergo oocyte cryopreservation. Women of childbearing potential must have a negative pregnancy test within 3 days prior to the first administration. (6) ECOG performance status of 0–1.

Exclusion criteria

Exclusion criteria: (1) Pregnant or breastfeeding patients. (2) Patients with impaired renal function, defined as a creatinine clearance < 40 mL/min. (3) Patients with concurrent primary malignant tumors. (4) Patients who have not signed the informed consent form or are unable to comply with study procedures. (5) ECOG performance status = 2. (6) Any other condition deemed unsuitable for study participation by the investigator.

Design outcomes

Primary

MeasureTime frame
maximum standardized uptake;Specificity;Sensitivity;Accuracy;

Secondary

MeasureTime frame
mean standardized uptake;

Countries

China

Contacts

Public ContactYueqi Wang

West China Hospital of Sichuan University

wangyue71992@163.com+86 173 8182 7671

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026