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Oxygen Therapy for Retinal Ischemia

Phase 4
Withdrawn
Conditions
Retinal Ischemia
Interventions
Drug: Hyperoxia
Registration Number
NCT03730779
Lead Sponsor
Beth Israel Deaconess Medical Center
Brief Summary

The investigators will be using nocturnal normobaric hyperoxia therapy in patients with diagnoses of conditions related to retinal ischemia.

Detailed Description

Patients who receive a diagnosis of a condition relate to retinal ischemia and who pass the eligibility criteria will receive an oxygen concentrator to use at home. They will report back in follow up monthly for three to six months.

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • Diagnosis of retinal-ischemia related condition
Exclusion Criteria
  • Complicating other ocular condition
  • History of smoking or lung conditions

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
O2 recievingHyperoxiaPatients who receive hyperoxia
Primary Outcome Measures
NameTimeMethod
Macula Edema6 months

Amount of ME present, as measured by OCT

Best Corrected Visual Acuity6 months

Best Corrected Visual Acuity as measured by ETDRS chart

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Beth Israel Deaconess Medical Center

🇺🇸

Boston, Massachusetts, United States

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