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The Effect of Transcorneal Stimulation in Cases of Central Retinal Artery Occlusion Using a New Waveform

NCT00802698 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 5

Last updated 2024-05-30

No results posted yet for this study

Summary

The purpose of this study is to describe the effect of transcorneal electrical stimulation (TES) with a non conventional biphasic bipolar waveform in central retinal artery occlusion

Conditions

  • Central Retinal Artery Occlusion

Interventions

DEVICE

Transcorneal electric stimulation

central artery occlusion

DEVICE

Transcorneal stimulation

new waveform

DEVICE

transcorneal electric stimulation

Novel waveform central artery occlusion

Sponsors & Collaborators

  • Asociación para Evitar la Ceguera en México

    lead OTHER

Principal Investigators

  • Miriam Jessica Lopez-Miranda, MD · Asociación para Evitar la Ceguera en México

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
50 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-04-30
Primary Completion
2008-04-30
Completion
2008-04-30

Countries

  • Mexico

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00802698 on ClinicalTrials.gov