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A Multimodal Study on Postoperative Changes in Visual Perceptual Function and Brain Activity in Cataract Patients

A Multimodal Study on Postoperative Changes in Visual Perceptual Function and Brain Activity in Cataract Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600118935
Enrollment
Unknown
Registered
2026-02-12
Start date
2026-02-12
Completion date
Unknown
Last updated
2026-02-16

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

Conditions

cataract

Interventions

cataract patients:None

Sponsors

Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 85 Years

Inclusion criteria

Inclusion criteria: Patients 1.Age 50 to 85 years (including 50 and 85 years), no gender restrictions; 2.Meets diagnostic criteria for bilateral cataracts; 3.Patients scheduled for bilateral phacoemulsification with intraocular lens implantation; 4.Able and willing to comply with all follow-up plans; 5.Voluntarily agree to participate in this study and provide written informed consent, unless informed consent is waived with approval from the ethics committee; Healthy Controls 1. Age 50–85 years (including 50 and 85), no gender restrictions; 2. Able and willing to comply with all follow-up plans; 3. Voluntarily agree to participate in this study and provide written informed consent, unless informed consent can be waived with the approval of the Ethics Committee.

Exclusion criteria

Exclusion criteria: 1.Systemic diseases that may affect postoperative outcomes, such as patients with unstable blood glucose control in diabetes; 2.Amblyopia, strabismus, glaucoma, corneal diseases, severe retinal diseases, and other ocular conditions that may compromise postoperative results; 3.History of ocular trauma or prior ocular surgeries that may confound observation findings; 4.Pregnant or lactating women; 5.Current or past history of traumatic brain injury, cerebrovascular disease (e.g., stroke), neurological disorders (e.g., epilepsy, Alzheimer's disease, Parkinson's disease), or psychiatric conditions (e.g., depression, schizophrenia); 6.History of alcohol dependence or substance abuse; 7.Presence of depressive symptoms, intellectual impairment, dementia symptoms, or sleep disorder symptoms; 8.Working memory capacity below 3 or inability to complete working memory tasks; 9.Claustrophobia or metallic implants that do not meet MRI safety standards; 10.Inability to comply with follow-up visits as directed; 11.Other circumstances where the investigator determines the patient is unsuitable for enrollment;

Design outcomes

Primary

MeasureTime frame
Changes in the connectivity of visual cortex, white matter fiber tracts, and spontaneous brain network fluctuations 7-30 days and 90-120 days post-surgery compared to pre-surgery;changes in amplitude of evoked potentials from preoperative levels at 7-30 days and 90-120 days postoperatively;

Secondary

MeasureTime frame
Changes in visual acuity, subjective refraction, intraocular pressure, slit-lamp examination, and iTrace examination results compared to pre-operation;

Countries

China

Contacts

Public ContactGuo Tao

Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine

guotao9@hotmail.com+86 21 2327 1699

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026