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Post-Radioiodine Graves' Management: The PRAGMA-Study

POST-RADIOIODINE GRAVES' MANAGEMENT

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01885533
Acronym
PRAGMA
Enrollment
803
Registered
2013-06-25
Start date
2013-03-31
Completion date
2015-12-31
Last updated
2017-03-30

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

Conditions

Graves' Disease

Keywords

Graves' disease, radioiodine, thyroid, hypothyroidism, Graves' orbitopathy

Brief summary

Thyroid dysfunction following radioiodine for Graves' disease is common, potentially detrimental and avoidable. A variety of clinical strategies are employed in the post-radioiodine era util the patient is on a stable thyroid hormone replacement regimen, which include the use of anti-thyroid drugs, antithyroid drugs with thyroxine, early thyroxine replacement and watchful monitoring until the onset of hypothyroidism. Which of these is most effective in avoiding dysthyroidism, is unknown. This study aims to address this lack of evidence. It will focus on Graves' disease as this is the commonest cause of thyrotoxicosis and the commonest indication for RI therapy. It will provide an insight into potential strategies for improving important clinical outcomes.

Interventions

None listed

Sponsors

Cardiff and Vale University Health Board
CollaboratorOTHER_GOV
Royal Devon and Exeter NHS Foundation Trust
CollaboratorOTHER
Newcastle-upon-Tyne Hospitals NHS Trust
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Out-patients 18 years of age or over, who have given written informed consent to participate in the study * Diagnosed with Graves' disease * Received radioiodine for treatment of Graves' disease * Had a minimum of 12 months follow-up after RI * Most recent RI dose 5 years ago or less at the time of enrollment

Exclusion criteria

* Patients unable to give informed consent * Age 17 years or younger * Cause of thyrotoxicosis other than Graves' disease * Patients who have had more than one dose of radioiodine can only be included in the study once, using data pertaining to their most recent treatment episode. * Patients who might not adequately understand verbal explanations or written information given in English, or who have special communication needs

Design outcomes

Primary

MeasureTime frameDescription
Incidence of dysthyroidism post-RI between different post-RI management strategies employed by clinicians in the UK12 months post radio-iodineTo compare the incidence of dysthyroidism post-RI between different post-RI management strategies employed by clinicians in the UK: * anti-thyroid drugs before and /or after RI * anti-thyroid drugs with levothyroxine before and / or after RI * watchful monitoring post-RI and introduction of levothyroxine when needed.

Secondary

MeasureTime frame
Graves orbitopathy12 months post-radiodiodine
weight gain12 months
progression of Graves' orbitopathy12 months
patient satisfaction12 months

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026