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Visual Development Study in Children with Cataracts

Visual Development Study in Children with Cataracts

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600122248
Enrollment
Unknown
Registered
2026-04-10
Start date
2026-04-15
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Congenital Cataract or Developmental Cataract

Interventions

Postoperative Pediatric Cataract Group:None
Control Group:None

Sponsors

Zhongshan Ophthalmic Center,Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 30 Years

Inclusion criteria

Inclusion criteria: Children with Congenital Cataracts 1. Age between 0 and 30 years; 2. History of bilateral congenital/developmental cataracts; 3. Underwent bilateral cataract extraction with intraocular lens implantation before the age of 8; 4. Regular use of corrective lenses postoperatively; 5. For minors, informed consent signed by parents or legal guardians. Normal Subjects 1. Age between 0 and 30 years; 2. For minors, informed consent signed by parents or legal guardians.

Exclusion criteria

Exclusion criteria: 1. Premature birth (<28 weeks); 2. Presence of eye diseases other than refractive errors (cataract, keratitis, corneal leukoma, aniridia, glaucoma, amblyopia) or systemic diseases (congenital heart disease, ischemic encephalopathy); 3. Family history of eye diseases (any congenital eye disease, such as congenital glaucoma, congenital aniridia); 4. History of ocular trauma; 5. Severe ocular comorbidities (small cornea, persistent hyperplastic primary vitreous, rubella, Lowe syndrome); 6. Difficulties in cooperating with examinations; 7. Currently participating in other clinical trials; 8. Considered by the investigator as unsuitable for this clinical trial for other reasons; 9. Pregnancy.

Design outcomes

Primary

MeasureTime frame
visual acuity;

Secondary

MeasureTime frame
Task?Based fMRI Activation Intensity/Extent;Contrast Sensitivity;

Countries

China

Contacts

Public ContactZitian Liu

Zhongshan Ophthalmic Center,Sun Yat-sen University

liuzt5@mail2.sysu.ed.cn+86 20 6661 0729

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026