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Evaluation of the efficacy of potassium iodide preparation for radioactive iodine therapy in Graves' disease

Evaluation of the efficacy of potassium iodide preparation for radioactive iodine therapy in Graves' disease - Evaluation of the efficacy of potassium iodide preparation for radioactive iodine therapy in Graves' disease

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000024893
Enrollment
24
Registered
2016-12-01
Start date
2011-05-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Graves&#39

Interventions

None listed

Sponsors

Yamashita thyroid and parathyroid clinic
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The inclusion criteria was defined as follows; more than 18 years old at RAIT.

Exclusion criteria

Exclusion criteria: The exclusion criteria was defined as follows; large goiter and/or experience of previous RAIT. The definition of large goiter in exclusion criteria was determined that estimated thyroid gland weight was more than 50 g.

Design outcomes

Primary

MeasureTime frame
variation of FT4 between before and at 4 days after discontinuation of methimazole (MMI) or KI between KI prepariton group and MMI preparation group

Secondary

MeasureTime frame
Radioactive iodine uptake before RAIT, thyroid gland weight, dose of administered 131-I, dose of 131-I based on thyroid gland weight, free thyroxine (FT4) at RAIT, thyroid function at one year after RAIT and thyroid gland weight at one year after RAIT between above two gruops

Countries

Japan

Contacts

Public ContactSeigo Tachibana

Yamashita thyroid and parathyroid clinic Endocrinology

sei.tac.thyroid@gmail.com092-281-1300

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026