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Phantom Eye Pain, Visual Function, Quality of Life, and Emotional Impact After Enucleation

Phantom Eye Pain, Visual Function, Quality of Life, and Emotional Impact After Enucleation

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500099842
Enrollment
Unknown
Registered
2025-03-31
Start date
2024-01-25
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Phantom eye pain

Interventions

Research group:None

Sponsors

Joint Shantou International Eye Center Of Shantou University And The Chinese University Of Hong Kong
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1. Volunteer and sign informed consent; 2. Over 18 years old; 3. Removal of one eye due to trauma or eye disease; 4. Clear consciousness and normal intelligence.

Exclusion criteria

Exclusion criteria: Exclusion criteria: 1. Refuse to sign informed consent to participate in the experiment; 2. Suffering from other eye diseases that seriously affect visual function, such as cataracts, glaucoma, and various fundus lesions 3. Combined with various severe facial deformities; 4. Combined with all kinds of serious systemic diseases, such as heart and brain diseases and mental disorders.

Design outcomes

Primary

MeasureTime frame
Emotion;Quality of life;—

Countries

China

Contacts

Public ContactTang Ruqing

Joint Shantou International Eye Center Of Shantou University And The Chinese University Of Hong Kong

trq@jsiec.org+86 138 2585 6841

Outcome results

None listed

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