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Use of 18F-PSMA-11 PET for Detection of Lesions in Iodine Refractory Thyroid Cancers

G

Ghent University Hospital (UZ)

Status and phase

Completed
Phase 2

Conditions

Thyroid Cancer

Treatments

Diagnostic Test: PET/CT scan F18-PSMA-11

Study type

Interventional

Funder types

Other

Identifiers

NCT05175404
BC-09501

Details and patient eligibility

About

Determine the diagnostic value of 18F-PSMA-11 in patients with iodine refractory thyroid cancer.

Enrollment

8 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient is 18 years or older.
  • Signed Informed Consent.
  • Subject is diagnosed with a histologically confirmed differentiated thyroid carcinoma, that is considered RAI refractory. There is evidence of persisting or recurrent disease, based on serum thyroglobulin levels and/or medical imaging.
  • Subject should have a routine clinical 18F-FDG PET/CT performed within two months prior to the study scan.
  • Female patients should be either post-menopausal, surgically sterile, or using highly effective contraceptives (methods that can achieve a failure rate of less than 1%: combined hormonal contraception, progestogen-only hormonal contraception associated with inhibition of ovulation, intrauterine device, intrauterine hormone-releasing system, bilateral tubal occlusion, vasectomized partner, sexual abstinence).

Exclusion criteria

  • Patient has a known other active malignancy.
  • Subject is potentially pregnant (urinary test can be performed in case of doubt) or breastfeeding.
  • Patient is mentally or legally incapacitated.

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

8 participants in 1 patient group

Overal Trial
Other group
Description:
only one arm in this trial
Treatment:
Diagnostic Test: PET/CT scan F18-PSMA-11

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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