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Iodine Uptake After a Low Iodine Diet (IULID)

Primary Purpose

Differentiated Thyroid Cancer

Status
Recruiting
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Low iodine diet
Sponsored by
University Medical Center Groningen
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Differentiated Thyroid Cancer focused on measuring Low iodine diet, Iodine uptake

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: 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 Exclusion Criteria: Age < 18 years Patients using amiodarone Patients receiving iodinated contrast < 3 months before the LID Pregnancy Patients prepared for ablation therapy with rhTSH Renal impairment, EGFR <30ml/min/1,73m2

Sites / Locations

  • UMCGRecruiting

Outcomes

Primary Outcome Measures

Iodine uptake
Difference in iodine uptake in percentage

Secondary Outcome Measures

Full Information

First Posted
October 25, 2022
Last Updated
September 18, 2023
Sponsor
University Medical Center Groningen
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1. Study Identification

Unique Protocol Identification Number
NCT05599139
Brief Title
Iodine Uptake After a Low Iodine Diet
Acronym
IULID
Official Title
The Uptake of Radioactive Iodine Before and After a Low Iodine Diet in Patients With Differentiated Thyroid Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 22, 2023 (Actual)
Primary Completion Date
September 30, 2024 (Anticipated)
Study Completion Date
August 31, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Medical Center Groningen

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
Rationale: Differentiated thyroid carcinoma (DTC) is the most common form of thyroid cancer. The initial treatment of DTC consists of a total thyroidectomy followed by ablation therapy with radioactive iodine (131I) which destroy residual thyroid (cancer) tissue. Before starting the (ablation) therapy with 131I, patients have to follow a low iodine diet (LID) reducing the iodine intake < 50 mcg per day. Depleting the overall iodine store in the body theoretically maximizes the expression of the sodium-iodine symporter (NIS). This increased NIS expression results in an increase of the uptake of 131I in remaining thyroid (cancer) cells during 131I therapy and therefore improves the ablation success rates. However, there is no prospective data to support this, merely some retrospective contradictionary data. Patients experience the strict adherence to LID as stressful, distasteful and overwhelming in combination with a new diagnosis of cancer and withdrawal from thyroid hormone. Besides, they are afraid to apply the LID inadequately, which complicates achieving a balanced diet, essential in cancer recovery. Objective: To compare the difference in thyroid uptake of a low dose radioactive iodine (10 MBq 123I or 37 MBq 123I), in DTC patients after thyroidectomy, before and after a LID of 7 days. Study design: observational, single center study performed in the University Medical Center Groningen (UMCG) Groningen, the Netherlands. Study population: Patients, men and women above the age of 18 years, with a histopathological confirmed diagnosis of DTC who will receive 131I ablation therapy and have to follow a LID according to the Dutch DTC guideline. Main study parameters/endpoints: The primary endpoint is the clinical relevant difference of a twofold uptake increase, in the thyroid remnant after thyroidectomy in DTC patients, a 10 MBq 123I or 37 MBq 123I tracer dose before and after a LID of 7 days. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Burden: Low risk patients (according to the Dutch DTC guideline) will receive 10 MBq 123I twice, followed by a thyroid uptake measurement and will have to collect their urine for 24 hours twice. High risk patients (according to the Dutch DTC guideline) will receive 10 MBq 123I once, followed by a thyroid uptake measurement and have to collect their urine for 24 hours twice. On the day of the first administration of 10 MBq 123I, 1 blood sample (5 ml) will be collected. Low risk patients have to make three additional site visits to the UMCG, high risk patients two additional site visits. Risks: The administration of two times 10 MBq will lead to an extra radiation exposure of 0,76 mSv for low risk patients and 0,38 mSv for high risk patients. Blood sampling carriers a negligible risk of a hematoma. The 24 hours urine collection is without additional risk for the patient or the lab technician. The note of the daily food intake is without additional risk for the patient. - Benefits: None, participants will participate based on altruistic motives.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Differentiated Thyroid Cancer
Keywords
Low iodine diet, Iodine uptake

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
25 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Behavioral
Intervention Name(s)
Low iodine diet
Intervention Description
Before ablation and possible subsequent therapy with 131I, patients have to follow a low iodine diet (LID), reducing the iodine intake < 50 mcg per day and thereby depleting the overall iodine store in the body.
Primary Outcome Measure Information:
Title
Iodine uptake
Description
Difference in iodine uptake in percentage
Time Frame
7 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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 Exclusion Criteria: Age < 18 years Patients using amiodarone Patients receiving iodinated contrast < 3 months before the LID Pregnancy Patients prepared for ablation therapy with rhTSH Renal impairment, EGFR <30ml/min/1,73m2
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Wouter Zandee, Dr.
Phone
+31503613731
Email
w.t.zandee@umcg.nl
First Name & Middle Initial & Last Name or Official Title & Degree
Mirthe Links, BSc.
Phone
+31503610973
Email
m.h.links@umcg.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wouter Zandee, Dr.
Organizational Affiliation
University Medical Center Groningen
Official's Role
Principal Investigator
Facility Information:
Facility Name
UMCG
City
Groningen
ZIP/Postal Code
9713GZ
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Wouter T Zandee, MD PhD
Phone
050 361 6161
Email
w.t.zandee@umcg.nl
First Name & Middle Initial & Last Name & Degree
Mirthe H Links, Bsc
Phone
050 361 6161
Email
m.h.links@umcg.nl

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
The IPD will not be available to other researchers as this is not included in the patient consent.
Links:
URL
https://www.jodiumarm.nl/
Description
Information website provided to all patients in the UMCG that have to follow a low iodine diet

Learn more about this trial

Iodine Uptake After a Low Iodine Diet

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