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NCT05591092Terminated

Radioiodine Planar and a SPECT/CT Imaging With Iodine-123 for Evaluation of Follicular Thyroid Nodules Prior to Surgery

Radioiodine Scanning for Pre-Surgical Evaluation of Follicular Thyroid Nodules

Source: ClinicalTrials.gov · Last updated 11 Aug 2026

Reason given: Slow accrual

Brief summary (registry, in English)

This study evaluates radioiodine planar and SPECT/CT imaging with iodine-123 in patients with follicular thyroid nodules prior to surgery. Because biopsy alone is not sufficient to distinguish between malignant follicular thyroid nodules and benign follicular thyroid nodules, patients with follicular thyroid lesions are referred for surgery for further evaluation. A non-invasive imaging method that can accurately determine malignancy in follicular thyroid nodules would be valuable in patient management and could potentially spare patients unnecessary surgery. Planar imagine uses a gamma camera to obtain 2D images and SPECT/CT imaging is a special type of CT scan in which a small amount of a radioactive drug is injected into a vein and a scanner is used to make detailed images of areas inside the body where the radioactive material is taken up by the tumor cells. Radioiodine planar and SPECT/CT imaging may be more accurate in distinguishing between benign follicular thyroid nodules and malignant follicular thyroid nodules to help reduce the need for surgery.

Status (registry)
Terminated
Study type
Observational
Enrollment
2 (actual)
First submitted
18 Oct 2022
Start date
10 Nov 2023
Primary completion date
21 Jan 2025
Lead sponsor
Mayo Clinic
NCT number
NCT05591092

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Current use of anti-thyroid medications (methimazole or propylthiouracyl)

Other illness

  • Recent iodinated contrast, including intravenous (IV) and oral CT contrast or interventional vascular or cardiac study (within 6 weeks)

Other

  • Hurthle cell adenoma
  • Current thyroid hormone supplementation
  • Less than 2 days after thyroid nodule FNA/biopsy
  • Presence of another nodule of similar size in the same area of thyroid lobe, which could impair localization of the nodule on SPECT/CT images
  • Less than 2/3 of normal thyroid tissue present in either thyroid lobe without nodules
  • Positive pregnancy test
  • All women who are breastfeeding

Who the study is looking for

  • Age \> 18 years
  • Any gender
  • Patients will have had no therapy for their thyroid nodule prior to enrollment
  • Negative urine pregnancy test within 48 hours before the administration of radiopharmaceutical in women of childbearing potential
  • Follicular neoplasm or suspicious of follicular neoplasm, cytopathology on biopsy of thyroid nodule
  • Any outside fine needle aspiration (FNA) reports are to be reviewed by a Mayo pathologist
  • Nodules 1-4 cm with solid appearance on ultrasound
  • Ultrasound images and report documented in medical record, including the size of the nodule and location (upper, mid or lower portion of the thyroid lobe)
  • At least 2/3 of either thyroid lobe without nodules should be present to allow for the measurement of uptake in unaffected thyroid tissue
  • Thyroid stimulating hormone (TSH) 0.3-3.0 mIU/L
  • Patient is scheduled or being considered for surgical resection of the nodule
  • I-123 planar and Single Photon Emission Computed Tomography (SPECT)/Computed Tomography (CT) can be scheduled at least 2 days after biopsy and before surgery

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Mayo Clinic in RochesterRochesterUnited StatesUnknown status

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