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A pilot study of intravitreal injection of methotrexate for intraocular lymphoma

A pilot study of intravitreal injection of methotrexate for intraocular lymphoma - A pilot study of intravitreal injection of methotrexate for intraocular lymphoma

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000021943
Enrollment
20
Registered
2016-04-20
Start date
2007-12-01
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

Intraocular lymphoma

Interventions

Perform intravitreal MTX (400 ug/100 ul) injection weekly for the eyes that were diagnosed as intraocular lymphoma until the lymphoma lesions are resolved.

Sponsors

Department of Ophthalmology & Visual Science, Tokyo Medical and Dental University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: A. Patients of intraocular lymphoma diagnosed according to the following criteria: 1) positive for characteristic ocular symptoms and findings of lymphoma 2) pathologically diagnosed as lymphoma 3) positive for IgH gene clonality detected by PCR assay or flow cytometry 1 with 2 or 3 B. Patients whose written informed consent can be obtained.

Exclusion criteria

Exclusion criteria: (1) Eyes with severe intraocular infectious disease (2) History of serious adverse reactions by methotrexate

Design outcomes

Primary

MeasureTime frame
Remission of the intraocular lesions, visual acuity, cytokine levels in intraocular fluids, and recurrence rate in two years.

Secondary

MeasureTime frame
Rate of adverse events, and relapse rate (central nerve system and other lesion)

Countries

Japan

Contacts

Public ContactHiroshi Takase

Tokyo Medical and Dental University Department of Ophthalmology & Visual Science

h.takase.oph@tmd.ac.jp+81-3-5803-5302

Outcome results

None listed

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