Thyroid Associated Ophthalmopathy

9

Review clinical trials related to Thyroid Associated Ophthalmopathy. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Sirolimus vs Corticosteroids in Treatment of Thyroid Eye Disease

The purpose of this study is to determine whether Sirolimus is more effective and burdened with less side effects than conventional treatment with corticosteroids in patients with active thyroid eye disease.

Participants needed: 60
Trial details
Phase: Phase 2Age: 18-80Biological sex: AllType: InterventionalSponsor: Haukeland University HospitalUpdated: Sep 22, 2025Locations: 1
Eligibility criteria

The participant want treatment for active thyroid eye disease and is willing to... [+9]

The participant dont want treatment for active thyroid eye disease or dont want... [+17]

Status: Recruiting

Construction and Application of Precise Diagnosis and Treatment System for Thyroid-associated Ophthalmopathy

This study aims to develop the deep learning-based system that integrates multimodal information to automatically diagnose, stage, and grade thyroid-associated ophthalmopathy (TAO), assist in treatment decision-making, and predict patient prognosis, thereby providing novel tools to support clinical management.

Participants needed: 500
Trial details
Age: 7-90Biological sex: AllType: ObservationalSponsor: Second Affiliated Hospital, School of Medicine, Zhejiang UniversityUpdated: Aug 15, 2025Locations: 1
Eligibility criteria

normal participants without eyelid disorders (control group) [+2]

participants with pupil or cornea disorders [+1]

Status: Recruiting

Establishment of Multiparametric Prediction Models for Moderate to SevereThyroid Associated Ophthalmopathy

Thyroid-associated ophthalmopathy (TAO) is an organ-specific autoimmune disease closely related to thyroid disease, which leads the incidence of orbital disease in adults and is the most common cause of diffuse toxic goiter (Graves disease, GD). The clinical manifestations of TAO are complex and varied. In severe cases, it may seriously impair visual function, affect daily life, and even cause corneal ulceration, perforation, and blindness. Therefore, a reasonable and effective treatment plan should be chosen according to the degree of TAO. The aim of this clinical study is to: 1. Found the new diagnostic markers or imaging sequences. 2. Establish and validate a multimodal and multiparameter prediction model for moderate to severe TAO.

Participants needed: 150
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Shanghai Changzheng HospitalUpdated: Jun 24, 2025Locations: 1
Eligibility criteria

According to the Bartley criteria,diagnosed TAO at our hospital after 2024/8/31 [+2]

Anticipated need for intervention due to sight-threatening complications or othe... [+6]

Status: Recruiting

A Study on the Combined Use of Tocilizumab and Flupentixol-Melitracen in the Treatment of Thyroid-Associated Ophthalmopathy

Thyroid-associated ophthalmopathy (TAO) is a serious, progressive, vision-threatening autoimmune disease that can be categorized into mild, moderate, and severe stages based on severity. The activity of TAO is commonly evaluated using the Clinical Activity Score (CAS). Tocilizumab serves as a second-line treatment option for patients with moderate to severe active TAO. Additionally, it is common for TAO patients to experience anxiety, which may exacerbate their condition and negatively impact prognosis. Therefore, we have designed this randomized controlled study to evaluate the impact of Flupentixol Melitracen (Lepan) on the treatment outcomes of participants receiving Tocilizumab (Actemra).

Participants needed: 60
Trial details
Phase: Phase 4Age: 18-80Biological sex: AllType: InterventionalSponsor: Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong UniversityUpdated: Apr 16, 2025Locations: 1
Eligibility criteria

Aged between 18 and 80 years (inclusive). [+4]

Severe cardiac, hepatic, or renal insufficiency (including myocardial ischemia o... [+9]

Status: Recruiting

Extension Study of Two Doses of Linsitinib in Subjects With Active, Moderate to Severe Thyroid Eye Disease (TED)

The overall study objective is to continue to assess the efficacy, safety, pharmacokinetics, and pharmacodynamics of linsitinib in subjects who were enrolled in the prior VGN-TED-301 through Week 24. These subjects include VGN-TED-301 Week 24 proptosis non-responders or subjects who relapse during the Follow-Up Period of VGN-TED-301.

Participants needed: 75
Trial details
Phase: Phase 2, Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Sling Therapeutics, Inc.Updated: Feb 25, 2025Locations: 2
Eligibility criteria

Subject who completed the 24-week double-mask period of VGN-TED-301 and are prop... [+3]

The exclusion criteria of protocol VGN-TED-301 also apply to this extension stud...

Status: Recruiting

Orbital Radiotherapy in Grave's Ophthalmopathy 1 Week vs 2 Weeks (OraGO-1 Trial)

Thyroid ophthalmopathy, also known as thyroid eye disease or Graves' ophthalmopathy, is a condition characterized by inflammation and swelling of the tissues around the eyes, often accompanied by protrusion of the eyeballs. This condition can lead to significant discomfort, visual disturbances, and in severe cases, permanent vision loss. Primary treatment modalities are intravenous methylprednisolone (IVMP) and other medications for patients with moderate to severe and active thyroid eye disease. In addition, external beam radiation therapy (ERT) is an another treatment option in combination with IVMP. Radiation therapy delivers targeted doses of ionizing radiation to the affected orbital tissues, effectively reducing inflammation. This approach is particularly beneficial for patients who may not respond adequately to steroid therapy alone or those who experience recurrent disease flares. This study will test the efficacy of a shortened treatment regimen comprising 5 sessions of ERT to a standard protocol of 10 treatments. The primary aim is to ascertain the effectiveness of shorted radiation treatment while improving patients' quality of life.

Participants needed: 68
Trial details
Phase: Phase 3Age: 18-70Biological sex: AllType: InterventionalSponsor: Janjira PetsuksiriUpdated: Dec 4, 2024Locations: 1
Eligibility criteria

Patient with active moderate to severe thyroid eye disease with a CAS > 4 with/... [+4]

Individuals with severe hypertension or diabetic retinopathy

Status: Recruiting

Treatment of Graves´ophthalmopathy with Simvastatin (GO-S)

In an investigator initiated multicenter trial (Malmö, Odense, Århus) the investigators aim at evaluating activity of Graves´ophthalmopathy (GO) and progress to severe GO in patients with mild to moderate Graves´ ophthalmopathy treated with simvastatin or no treatment.

Participants needed: 80
Trial details
Phase: Phase 3Age: 18-70Biological sex: AllType: InterventionalSponsor: Lund UniversityUpdated: Sep 25, 2024Locations: 1
Eligibility criteria

Age 18-70 years [+2]

Pregnancy or breast-feeding [+12]

Status: Recruiting

Multi-model Image of Doxycycline in TAO

This study aims to evaluate the efficacy of doxycycline treating Thyroid Associated Ophthalmopathy by multi-modal image.

Participants needed: 20
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: Sun Yat-sen UniversityUpdated: Nov 22, 2023Locations: 1
Eligibility criteria

Informed consent [+2]

Sight-threatening TAO with dysthyroid optic neuropathy [+2]

Status: Not yet recruiting

A Trial to Evaluate the Efficacy of Orbital Radiotherapy in Graves' Orbitopathy

Graves' orbitopathy (GO) is a disfiguring and disabling disease that profoundly impairs the quality of life of affected patients. High dose intravenous (iv) glucocorticoids (GC) (ivGC) is a well established, widely used treatment for active GO. The use of systemic glucocorticoids takes advantage from their immune suppressive and antiinflammatory actions, resulting in an overall beneficial effect ranging from \~35 to \~60% of patients in various studies. The intravenous route of administration has been shown to be superior to the oral route, both in terms of GO outcome and side effect profile. The combination of ivGC and orbital radiotherapy (OR) is used routinely in patients with moderate-severe, active GO, as a second-line treatment, as also recommended in the recent Guidelines published by the European Thyroid Association/European Group on Graves' Orbitopathy. Thus, the majority of studies have shown that OR increases the response rate to GC. Those studies were performed using oral GC, whereas it is not known whether OR potentiate also the effects of ivGC. The present study is aimed at determining whether OR potentiate the effects of ivGC in the treatment of moderately severe and active GO, in terms of GO outcome and quality of life. A possible extension of the study can be foreseen, aimed at investigating the very long time GO outcome.

Participants needed: 120
Trial details
Phase: Phase 4Age: 35-75Biological sex: AllType: InterventionalSponsor: University of PisaUpdated: Mar 15, 2023
Eligibility criteria

A diagnosis of Graves' disease based on the presence of hyperthyroidism (either... [+13]

Absence of Graves' hyperthyroidism (present or past) [+13]