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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04663451
Other study ID # 2019/435
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date September 11, 2020
Est. completion date May 2021

Study information

Verified date April 2021
Source Universitair Ziekenhuis Brussel
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Low RAIU in patients with hyperthyroidism represents a common obstacle in the treatment with RAI. Therefore, a higher dose of RAI must be administered to cure hyperthyroidism in these patients. If we treat patients with thiamazole before starting RAI treatment, serum TSH will rise and result in an increase in iodine uptake by the thyroid gland. By doing so, the dose of RAI to be administered might be lowered to achieve similar therapeutic efficacy. In the past, either calculated or fixed doses of 131I have been used to treat hyperthyroidism. The supposed advantage of a calculated dose compared to a fixed dose is the lowering of hypothyroidism frequency. However, various research papers have contradicted this statement. Antithyroid drugs and RAI therapy have been widely used in the past, either in combination, or independent from one another. This has been done primarily in older patients, to reduce the risk of exacerbation of hyperthyroid symptoms after initiation of RAI. The use of propylthiouracil has been shown to decrease the response rate after RAI due to radioprotective effects. The use of methimazole and carbimazole did not have a negative effect on treatment failure, as long as the medication was discontinued various days before RAI administration. Although this statement is contested in other studies. It is interesting to evaluate retrospective data of patients treated with RAI to evaluate prognostic factors of treatment respons and post RAI hypothyroidism.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 150
Est. completion date May 2021
Est. primary completion date November 24, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Hyperthyroid patients, either subclinical or overt, who have undergone RAI treatment in the period of 2005-2015. Exclusion Criteria: - Prior use of L-thyroxine - Prior thyroid surgery - Prior RAI treatment - Patients with thyroiditis

Study Design


Related Conditions & MeSH terms


Intervention

Radiation:
radioacive iodine therapy
Hyperthyroid patients who have undergone radioactive iodine treatment to cure them from their hyperthyroidism.

Locations

Country Name City State
Belgium Universitair Ziekenhuis Brussel Brussels

Sponsors (1)

Lead Sponsor Collaborator
Universitair Ziekenhuis Brussel

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary The proportion of patients in which hypothyroidism occurs The proportion of patients in which hypothyroidism occurs after radioiodine treatment Within 1 year after treatment
Primary The proportion of patients in which hypothyroidism occurs The proportion of patients in which hypothyroidism occurs after radioiodine treatment Between 1-2 years after treatment
Primary The proportion of patients in which hypothyroidism occurs The proportion of patients in which hypothyroidism occurs after radioiodine treatment Between 2-5 years after treatment