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Prospective study of the association between cognitive impairment and primary glaucoma

Prospective study of the association between cognitive impairment and primary glaucoma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500113920
Enrollment
Unknown
Registered
2025-12-04
Start date
2024-07-28
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Glaucoma is a group of diseases with characteristic optic atrophy and visual field defect, and pathological increase of intraocular pressure is the main risk factor. Primary glaucoma is a kind of glaucoma whose etiological mechanism is not fully understood. According to the state of the anterior chamber Angle when the intraocular pressure rises - closed or open, it can be divided into angle-closed

Interventions

Control group:None
Case group:None

Sponsors

Army Characteristic Medical Center, Chinese People's Liberation Army
Lead Sponsor

Eligibility

Sex/Gender
All
Age
55 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Inclusion criteria for the case group: (1) Age >=55 years; (2) Patients diagnosed with primary glaucoma based on the 2014 Expert Consensus on the Diagnosis and Treatment of Primary Glaucoma in China by the Glaucoma Subgroup of the Chinese Ophthalmological Society, meeting at least four of the following criteria: 1) Intraocular pressure (IOP) >=21 mmHg; 2) Cup-to-disc ratio (CDR) >=0.6 or interocular CDR difference >0.2; 3) RNFL defect; 4) Early visual field loss; (3) Uncorrected or best-corrected visual acuity >0.3, refractive error 0.3, refractive error <=+/-6D; (3) No history of major diseases or infectious diseases (including Hepatitis B, Hepatitis C, HIV, Syphilis); (4) Scheduled for cataract surgery and meeting surgical indications; (5) Voluntary participation in the study with signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with severe cognitive decline or inability to cooperate with examinations; 2. Patients with other vitreous or retinal diseases (including hereditary vitreoretinal degeneration, vitreous opacities, retinal vascular occlusion, arteriosclerosis, hematologic retinopathy, diabetic retinopathy, epiretinal membrane, retinal degeneration, and retinal dystrophy); 3. Patients with a history of intraocular surgery, including glaucoma surgery and non-glaucoma intraocular surgery; 4. Patients with ocular perforating or blunt trauma caused by intraocular foreign bodies, or secondary angle abnormalities or secondary glaucoma resulting from intraocular foreign bodies; 5. Patients with other neurodegenerative diseases or comorbidities that interfere with spinal cord assessment, such as multiple sclerosis, amyotrophic lateral sclerosis, vitamin B12 deficiency, and progressive spastic paraparesis (including hereditary spastic paraparesis); 6. Patients who have not provided informed consent.

Design outcomes

Primary

MeasureTime frame
Score of Mini-mental state examination;

Secondary

MeasureTime frame
Eyesight;Visual field;Results of photopic negative response(PhNR);Intraocular pressure;OCT outcome;Basic demographic and clinical characteristics of participants (name, gender, age, time of glaucoma diagnosis, type of glaucoma, etc.);

Countries

China

Contacts

Public ContactLiu,Ting

Army Characteristic Medical Center, Chinese People's Liberation Army

tingliu1597@126.com+86 15823486785

Outcome results

None listed

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