Perioperative Specimen Imaging Using High-resolution 18F-FDG-PET-CT During Thoracic Surgery: a Pilot Study
Recruiting now · Not applicable
Conditions studied: Lung Neoplasms, PET-CT Specimen Imager
In brief
In this pilot study the investigators propose the intraoperative use of a high-resolution PET-CT imaging system which can assess resection margins and lymph node status in the operating room. This will allow for a faster and stepwise assessment (estimated to be under 10 minutes per specimen), enabling the surgeon to decide on subsequent surgical steps after each previous assessment.
Key facts
- Study ID
- NCT05693363
- Run by
- University Hospital, Ghent
- People needed
- 40
- Starts
- 2024-01-01
- Expected to finish
- 2025-07-31
- Last updated by the study team
- 2025-01-15
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patient is 18 years of age or older.
- Patient with suspected or confirmed lung malignancies
- Patient is indicated to undergo thoracic surgery.
- Patient is estimated to be compliant for study participation by the investigator.
- Patient has freely given his/her informed consent to participate in this study.
You may not qualify if…
- Patient has general or local contra-indications for thoracic surgery.
- Patient has active infection.
- Blood glucose level over 200 mg/dL on the day of surgery.
- Pregnancy or lactation.
- Patient participated in other clinical studies with radiation exposure of more than 1 mSv in the past year
Where it is running
- University Hospital Ghent — Ghent, Belgium (enrolling)
Full record on ClinicalTrials.gov
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