ClinicalTrials.gg
WithdrawnNCT06024668Updated Jul 9, 2026

Simulated Walking With Multiplexing Prism for Field Expansion in Monocular Vision

An interventional study of Multiplexing Prism in One Eye Blindness, Blind Left Eye and Blind Right Eye, sponsored by Massachusetts Eye and Ear Infirmary. Withdrawn at 1 site in United States. Open to participants aged 16 Years and older. Per ClinicalTrials.gov, last updated 2026-07-09.

Sponsored by Massachusetts Eye and Ear Infirmary · Not applicable, Interventional, and Basic science

Why this study was withdrawn
Investigators left the research institute.
Phase
Not applicable
Study type
Interventional
Enrollment
0
Allocation
Not applicable
Ages
16 Years and older
Sex
All
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Study summary

The investigators are developing an assistive device, known as multiplexing prism that expands the field of view for individuals with acquired monocular vision (loss of an eye). The investigators will test the efficacy of the prism in improving the detection of colliding pedestrians during a simulated walking task.

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Conditions studied

  • One Eye Blindness
  • Blind Left Eye
  • Blind Right Eye

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Keywords

  • Simulated Walking
  • Collision
  • Field Expansion
  • One eye blindness
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In context

Blindness

144 studies on the registry are indexed under Blindness; 33 are open to participants now.

Browse Blindness studies →

Lead sponsor

Massachusetts Eye and Ear Infirmary is the lead sponsor of 100 studies on the registry; 23 are open to participants now.

Of its 13 completed or terminated interventional studies of FDA-regulated products, 7 (54%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
16 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • No medical health issues such as seizures, motor movements problem
  • Loss of vision in one eye (less than 20/200) for >1 year
  • Visual acuity of the seeing eye: Better than 20/32 visual acuity with correction
  • No visual field defect in the seeing eye (nasal field of at least >45degree)

Exclusion criteria

Exclusion Criteria:

  • Patients with any physical or mental disabilities, including cognitive dysfunction, balance problems, or other deficits that could impair their ability to respond to the stimuli presented in this study will be excluded
  • Any person with a history (such as pacemaker use or photosensitive epilepsy)
  • Any person with motor movements problem (e.g., unable to use extremities)
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Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • Experimental
    Detection of colliding pedestrian

    Participants will perform a simulated walking task in which surrounding pedestrians will walk towards and make a collision. Participants will respond by pressing buttons to indicate the direction of the colliding pedestrians. Participants will perform the task with and without the multiplexing prism in random orders.

    Device: Multiplexing Prism

Interventions

  • DeviceMultiplexing Prism

    Multiplexing prism is designed for spatial vision multiplexing. It allows partial light transmission through the prism allow the observer to simultaneously see the physical world through the prism and see the "shifted view" from the non-seeing side. It is developed to expand the field of view of individuals with just one eye.

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What researchers measure

Primary outcomes

  1. Mean response time to detect colliding pedestrian

    The investigators will compare the mean response time to detect colliding pedestrians coming from the nasal (same side as the blind eye) and temporal (same side as the seeing eye) visual field with and without multiplexing prism. The comparison will be made between these four: Nasal without prism, Temporal without prism, Nasal with prism, and Temporal with prism.

    Time frame: Approximately 3 sessions, up to 3 hours for each session, any time within 4 month period

Secondary outcomes

  1. Pedestrian Detection Rate

    The investigators will measure the rate of correct detection rate of colliding pedestrians in the nasal (same side as the blind eye) and temporal (same side as the seeing eye) with and without multiplexing prism. Comparisons will be made for these: nasal without prism, temporal without prism, nasal with prism,and temporal with prism.

    Time frame: Approximately 3 sessions, up to 3 hours for each session, any time within 4 month period

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Study locations

1 site
  • Schepens Eye Research Institute
    Boston, Massachusetts 02114, United States
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References and documents

Publications

  • Jung JH, Castle R, Kurukuti NM, Manda S, Peli E. Field Expansion with Multiplexing Prism Glasses Improves Pedestrian Detection for Acquired Monocular Vision. Transl Vis Sci Technol. 2020 Jul 23;9(8):35. doi: 10.1167/tvst.9.8.35. eCollection 2020 Jul. PubMed 32855881 ↗
  • Jung JH, Peli E. Field Expansion for Acquired Monocular Vision Using a Multiplexing Prism. Optom Vis Sci. 2018 Sep;95(9):814-828. doi: 10.1097/OPX.0000000000001277. PubMed 30169357 ↗
  • Jung JH, Peli E. No Useful Field Expansion with Full-field Prisms. Optom Vis Sci. 2018 Sep;95(9):805-813. doi: 10.1097/OPX.0000000000001271. PubMed 30169356 ↗

Individual participant data

Plan to share: No

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Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Aug 2024 to primary completion in Dec 2024, 4 months.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 29, 2023
First posted
Sep 6, 2023
StartActual
Aug 4, 2024
Primary completionActual
Dec 31, 2024
CompletionActual
Jan 1, 2025
Last update
Jul 9, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06024668
Responsible party
Eli Peli (Senior Scientist, Massachusetts Eye and Ear Infirmary) — Principal investigator
First posted
Sep 6, 2023
Start date
Aug 4, 2024
Primary completion
Dec 31, 2024
Completion
Jan 1, 2025
Last update
Jul 9, 2026

Study contacts

Eli Peli, OD
principal investigator · Schepens Eye Research Institute

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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