Clinical trial registry record

Evaluation of New Head-mounted Visual Aids Among Patients With Low Vision

A registered study indexed because it matched monitored longevity research terms. Registry status: Unknown. Registration does not establish safety or effectiveness.

Plain-language guide

Five questions to ask about this record

What this is
A clinical study registration, not a result or recommendation.
Why it may matter
The registry currently reports Unknown.
Evidence
Registered phase not reported study.
Main limitation
Registration does not prove that the intervention works, is safe, or is available to you.
What changed
Registry metadata was last updated October 11, 2023.
Where to verify
Open the primary registry below for eligibility, locations, contacts, and current status.
Registry ID
NCT06076720
Last registry update
October 11, 2023
Status
Unknown
Phase
Phase not reported
Sponsor
Zhongshan Ophthalmic Center, Sun Yat-sen University
Enrollment
50
Countries
China
Match confidence
100%
Source feed
ClinicalTrials.gov
Automated source synopsis

A registered study indexed because it matched monitored longevity research terms. Registry status: Unknown. Registration does not establish safety or effectiveness.

Evidence snapshot

What the source actually supports

Evidence stage
Phase not reported
Study design
NA · SINGLE GROUP · TREATMENT · NONE
Evidence population
Human clinical study registration
Participants
50
Population
ALL · 10 Years to 80 Years
Duration
2023-10-10 to 2024-10-10
Intervention
New head-mounted visual aids
Comparator
Not reported
Outcomes measured
Comparison of changes in the Glaucoma Visual Functioning Questionnaire-40 (GVFQ-40) scores at different time points — 8…; Comparison of changes in the National Eye Institute-Visual Function Questionnaire-25 (NEI VFQ-25) scores at different t…; Comparison of changes in the Low Vision Quality-of-Life Questionnaire (LVQOL) scores at different time points — 8 weeks…; Comparison of changes in visual acuity at different time points — 8 weeks after intervention; Comparison of changes in contrast sensitivity at different time points — 8 weeks after intervention; Comparison of changes in kinetic visual field at different time points — 8 weeks after intervention; Comparison of changes in functional magnetic resonance imaging (MRI) at different time points — 6 months after interven…; Comparison of changes in mobility test at different time points — 8 weeks after intervention; Comparison of changes in visual scanning test at different time points — 8 weeks after intervention
Reported result
No reusable finding-level result is available in this record.

Main limitationThis is a study registration. No reusable structured result is available here, so it cannot show whether the intervention worked or was safe.

Safety and approvalEligibility, adverse-event details, and clinical decisions must be checked in the official registry and with qualified clinicians. Trial registration is not regulatory approval and does not establish that an intervention is available.

Source supportStructured registry protocol metadata; no finding-level conclusion is generated.

Trial stage · Phase not reportedA trial phase describes development stage; it does not establish a positive result.
Phase 1Phase 2Phase 3Phase 4

Registration and recruitment status do not establish safety, efficacy, or regulatory approval.

Why this record appears here · 100% topic match

The title, summary, or source keywords matched one or more topics followed by immortal.life. A higher percentage means a stronger topic match; it does not rate safety, effectiveness, or study quality.

  • Vision ageing · 100%Abstract contains controlled term: age-related macular degeneration. Source terminology contains: age-related macular degeneration. Abstract supplies longevity context: age-related. Study type is explicitly identified as INTERVENTIONAL.

Automated source check 100% · update recency 65%. These figures help sort records; they are not medical ratings.

vision aging
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