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NCT Number: NCT07400757

Statin and Vitamin D Treatment in Patients With Thyroid Eye Disease

The goal of this clinical trial is to learn whether statin therapy and vitamin D supplementation can modify disease activity in patients with active thyroid eye disease. The study will also evaluate the safety of these treatments. The main questions it aims to answer are:

* Does statin therapy change disease activity, as measured by changes in the Clinical Activity Score (CAS) and proptosis? * Does vitamin D supplementation change disease activity in patients with active thyroid eye disease? * Does combined treatment with statin and vitamin D produce different effects compared with either treatment alone or standard care? * What adverse events occur during treatment?

Researchers will compare four groups: standard care alone, statin therapy plus standard care, vitamin D supplementation plus standard care, and combined statin and vitamin D therapy plus standard care.

Participants will:

* Be randomly assigned to one of four treatment groups * Receive the assigned treatment for 24 weeks * Attend clinic visits for clinical assessments and blood tests at baseline and at 24 weeks * Be followed through medical record review for up to three years after completion of the intervention

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Key information

Age range

20 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Taipei Veterans General Hospital

Taipei, Taiwan, 11217

Location status: Recruiting

Location contact

Chin-Sung Kuo, MD, PhD

CONTACT

[email protected]

886-2-28757513

About this study

Thyroid eye disease (TED) is an autoimmune inflammatory disorder commonly associated with Graves' disease. The disease typically follows an active inflammatory phase, characterized by orbital inflammation, pain, redness, swelling, and progression of eye protrusion, followed by an inactive fibrotic phase with more permanent structural changes. Early intervention during the active phase is critical to reduce disease severity and prevent long-term functional and cosmetic complications.

Current treatments for active TED primarily focus on immunosuppression, such as systemic corticosteroids or other immunomodulatory therapies. However, these treatments may be associated with significant side effects and variable treatment responses. Therefore, there is an unmet need for adjunctive therapies with favorable safety profiles that may modify disease activity and change outcomes in patients with active TED.

Recent observational studies have suggested that statin use is associated with a lower risk of developing thyroid eye disease and a reduced severity of disease manifestations. These potential benefits appear to be independent of cholesterol-lowering effects and may be related to the anti-inflammatory and immunomodulatory properties of statins. In addition, vitamin D deficiency has been frequently observed in patients with TED, and vitamin D is known to play a role in immune regulation and inflammatory control. Experimental and clinical studies suggest that vitamin D supplementation may modulate autoimmune activity and modify inflammatory responses.

Despite these findings, there is limited prospective clinical trial evidence evaluating the effects of statin therapy and vitamin D supplementation in patients with active TED. This study is designed as a randomized, open-label, 2×2 factorial clinical trial to evaluate the individual and combined effects of statin therapy and vitamin D supplementation on disease activity in patients with active TED.

Eligible participants with active TED will be randomly assigned to one of four groups: standard care alone, standard care plus statin therapy, standard care plus vitamin D supplementation, or standard care plus combined statin and vitamin D therapy. The intervention period will last for 24 weeks. Statin therapy consists of oral atorvastatin 20 mg once daily, and vitamin D supplementation consists of oral vitamin D at a daily dose of 1400 IU.

The primary outcomes of the study include changes in the Clinical Activity Score (CAS), responder rate defined as a ≥2-point change in Clinical Activity Score (CAS), changes in proptosis measured by Hertel exophthalmometry, and changes in thyroid-stimulating immunoglobulin (TSI) levels from baseline to 24 weeks. Secondary outcomes include changes in thyroid function, lipid profiles, blood glucose levels, and the use of thyroid-related medications and systemic corticosteroids during the intervention period.

Safety assessments will be conducted throughout the study by monitoring clinical symptoms, laboratory parameters, and reported adverse events. After completion of the 24-week intervention, participants will return to standard care and will be followed through medical record review for up to three years to observe long-term disease activity outcomes.

This study aims to provide prospective clinical evidence regarding the potential role of statin therapy and vitamin D supplementation as adjunctive treatments for active thyroid eye disease.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults aged 20 years or older
  • Diagnosis of active thyroid eye disease with a Clinical Activity Score (CAS) of 3 or higher
  • Low-density lipoprotein cholesterol (LDL-C) level of 100 mg/dL or higher

Exclusion criteria

  • Prior orbital radiotherapy or orbital surgery for thyroid eye disease
  • Use of statins or high-dose vitamin D supplementation (greater than 400 IU per day) within 3 months prior to enrollment
  • Pregnancy
  • Severe renal impairment, defined as an estimated glomerular filtration rate (eGFR) less than 30 mL/min/1.73 m²

Treatment and study plan

atorvastatin (Lipitor)

Drug

Oral atorvastatin 20 mg administered once daily for 24 weeks.

Vitamin D

Dietary Supplement

Oral vitamin D supplementation at a dose of 1400 IU administered once daily for 24 weeks.

Primary outcomes

  1. Change in Clinical Activity Score (CAS)

    Time frame: Baseline to 24 weeks

    The Clinical Activity Score (CAS; range 0-7, with higher scores indicating greater disease activity)

  2. Change in Thyroid Eye Disease Activity (Responder Analysis)

    Time frame: Baseline to 24 weeks

    Proportion of participants achieving a ≥2-point change in the Clinical Activity Score (CAS; range 0-7, with higher scores indicating greater disease activity)

  3. Change in Proptosis

    Time frame: Baseline to 24 weeks

    Change in proptosis measured by Hertel exophthalmometry

  4. Change in Thyroid-Stimulating Immunoglobulin (TSI)

    Time frame: Baseline to 24 weeks

    Change in serum thyroid-stimulating immunoglobulin (TSI) levels

Secondary outcomes

  1. Change in Thyroid Function

    Time frame: Baseline to 24 weeks

    Change in thyroid function parameters (TSH, free T4, free T3)

  2. Change in Lipid Profile

    Time frame: Baseline to 24 weeks

    Change in lipid parameters, including low-density lipoprotein cholesterol (LDL-C)

  3. Change in Blood Glucose

    Time frame: Baseline to 24 weeks

    Change in blood glucose levels

  4. Concomitant Medication Use

    Time frame: Baseline to 24 weeks

    Use of thyroid-related medications and systemic corticosteroids during the intervention period

Study contacts

Contact information is provided by the study sponsor or research team.

Chin-Sung Kuo, MD, PhD

CONTACT

[email protected]

886-2-28757513

Sponsors and collaborators

Lead sponsor

Taipei Veterans General Hospital, Taiwan

Other Gov

Registry information

Official study title

The Role of Statin and Vitamin D for the Treatment of Thyroid Eye Disease

Important dates

Study start
2026
Primary completion
2029
Study completion
2032
First posted
Feb 10, 2026
Registry last updated
Apr 30, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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