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NCT05599139Recruiting

Iodine Uptake After a Low Iodine Diet

The Uptake of Radioactive Iodine Before and After a Low Iodine Diet in Patients With Differentiated Thyroid Carcinoma

Source: ClinicalTrials.gov · Last updated 6 Feb 2026

Brief summary (registry, in English)

The goal of this clinical trial is to compare the difference in thyroid uptake of a low dose radioactive iodine (10 MBq 123-I or 37 MBq 123-I) in athyreotic patients with differentiated thyroid carcinoma before and after a low iodine diet (LID) of 7 days. The main question it aims to answer is: • What is the difference in iodine uptake before and after a LID of 7 days? Uptake of a low dose of 123-iodine will be measured in participants before and after a low iodine diet of 7 days. Researchers will compare the uptake (%) before and after the LID.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
25 (estimated)
First submitted
25 Oct 2022
Start date
22 Feb 2023
Primary completion date
30 Mar 2026
Lead sponsor
University Medical Center Groningen
NCT number
NCT05599139

What you commit to

  • Study type: Interventional
  • Planned participants: 25
  • From 22 Feb 2023 to the primary completion date, 30 Mar 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

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

Prior treatment

  • Patients receiving iodinated contrast \< 3 months before the LID
  • Patients prepared for ablation therapy with rhTSH

Lab values

  • Renal impairment, EGFR \<30ml/min/1,73m2

Age

  • Age \< 18 years

Other

  • Patients using amiodarone
  • Pregnancy

Who the study is looking for

  • Patients, men and women above the age of 18 years, have to be diagnosed with DTC and have to follow a LID prior to the 131I ablation therapy according to the Dutch DTC guideline
  • Patients have to be fit to adhere to the study protocol
  • Patients have to be able to read and understand the Dutch language

Age in the registry: 18 years to 75 years · 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
UMCG
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GroningenNetherlandsRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.