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Bimatoprost as a Treatment for Graves' Orbitopathy

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Johns Hopkins University

Status and phase

Enrolling
Early Phase 1

Conditions

Graves Ophthalmopathy

Treatments

Drug: Bimatoprost Ophthalmic

Study type

Interventional

Funder types

Other

Identifiers

NCT03708627
IRB00294393

Details and patient eligibility

About

Testing whether Bimatoprost, a topical eye drop used for glaucoma, can be used to induce periorbital fat atrophy in patients with Graves' disease

Enrollment

3 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria: Graves' Ophthalmopathy with Exophthalmos/Proptosis -

Exclusion Criteria: Active Graves Disease, Currently pregnant, Taking Steroids

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

3 participants in 2 patient groups

Bimatoprost in more proptotic eye
Experimental group
Description:
Patients instill Bimatoprost in their more proptotic eye one nightly
Treatment:
Drug: Bimatoprost Ophthalmic
Control
No Intervention group
Description:
Bimatoprost is not instilled in the patient's fellow eye

Trial contacts and locations

1

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Central trial contact

Emily Li, MD

Data sourced from clinicaltrials.gov

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