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Study for therapeutic effect on intra-orbital low doses rituximab injection for thyroid-associated orbitopathy and idiopathic orbital inflammatory syndrome

Study for therapeutic effect on intra-orbital low doses rituximab injection for thyroid-associated orbitopathy and idiopathic orbital inflammatory syndrome

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100043287
Enrollment
Unknown
Registered
2021-02-09
Start date
2021-02-01
Completion date
Unknown
Last updated
2022-11-14

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

Conditions

thyroid-associated orbitopathy and idiopathic orbital inflammatory syndrome

Interventions

Group A:rituximab 10mg
Group B:rituximab 20mg
Group C:rituximab 10mg

Sponsors

Department of Ophthalmology, Tangdu Hospital, Fourth Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Patients clearly diagnosed as IOID or TAO. 2. The age ranges from 6 to 75 years old, regardless of gender. 3. Agree to join the group and sign a written informed consent form. 4. Exclude patients from the criteria. 5. Those who have good compliance and agree to take drugs and accept evaluation in accordance with the requirements of the research program.

Exclusion criteria

Exclusion criteria: 1. Complicated with other orbital diseases. 2. Patients with hematological diseases who are using hormones or similar experimental drugs. 3. Patients who have participated in clinical trials of other drugs or at the same time within 3 months before treatment. 4. Women during pregnancy, lactation, or women of childbearing age who are willing to become pregnant. 5. People who are allergic to rituximab or allergic to rituximab. 6. Alcoholism, drug addicts or other uncontrollable neuropsychiatric disorders are not suitable for drug testing. 7. The researchers believe that it is not appropriate for patients to participate in other conditions of this trial.

Design outcomes

Primary

MeasureTime frame
CAS;

Countries

China

Contacts

Public ContactYang-Jun Li

Tangdu Hospital, the Fourth Military Medical University

liyjun1969@126.com+86 15029226669

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026