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Effectiveness of binasal occlusion in vision impairment induced by acquired brain injury: a hospital-based case control study

Effectiveness of binasal occlusion in vision impairment induced by acquired brain injury: a hospital-based case control study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300074777
Enrollment
Unknown
Registered
2023-08-16
Start date
2023-08-20
Completion date
Unknown
Last updated
2023-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Visual dysfunction associated with acquired brain injury

Interventions

test group:Binasal occlusion therapy
control group:NA

Sponsors

China Rehabilitation Research Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: ?Patients with acquired brain injury; ? Selected patients are older than 18 years old and younger than 70 years old, and no fundus lesions are found in preoperative or postoperative examination; ?The preoperative diopter of the selected patients is less than -6.00D, the eye axis is =22mm and =26mm, and the average corneal curvature is =41D and =47D; ?Patients voluntarily accept the treatment and sign the informed consent, and patients with cognitive impairment can be signed by their family members.

Exclusion criteria

Exclusion criteria: ?Patients had a medical history of strabismus before trauma; ? There is a history of eye surgery; ?With optic atrophy, diabetic fundus disease, high myopia, glaucoma and age-related macular degeneration; ?Combined with severe insufficiency of vital organs; ?Patients with severe disturbance of consciousness. ? 88 / 5,000 ?Patients had a medical history of strabismus before trauma; ? There is a history of eye surgery; ?With optic atrophy, diabetic fundus disease, high myopia, glaucoma and age-related macular degeneration; ?Combined with severe insufficiency of vital organs; ?Patients with severe disturbance of consciousness.

Design outcomes

Primary

MeasureTime frame
vision;intraocular pressure;eye position;Near Infrared Functional Imaging;

Secondary

MeasureTime frame
functional magnetic resonance imaging;visual evoked potential;

Countries

China

Contacts

Public ContactZHOU JIE

China Rehabilitation Research Center

ashily.hi@163.com+86 136 0137 2859

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026