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Efficacy and safety studies on fovea-sparing internal limiting membrane peeling for myopic foveoschisis

Efficacy and safety studies on fovea-sparing internal limiting membrane peeling for myopic foveoschisis

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000036087
Enrollment
Unknown
Registered
2020-08-21
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-09-07

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

Conditions

myopic foveoschisis

Interventions

Case series:fovea-sparing internal limiting membrane peeling

Sponsors

Joint Shantou International Eye Center of Shantou University and the Chinese University of Hong Kong
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: patients with myopic foveoschisis receiving surgical treatment

Exclusion criteria

Exclusion criteria: 1. Accompany with other diseases which decrease visual acuity, such macular hole, retinal detachment or glaucoma; 2. patients with silicon oil tamponade during surgery.

Design outcomes

Primary

MeasureTime frame
best corrected visual acuity;incidence of Iatrogenic macular hole formation;

Countries

China

Contacts

Public ContactZheng Dezhi

Joint Shantou International Eye Center of Shantou University and the Chinese University of Hong Kong

15989849662@163.com+86 15989849662

Outcome results

None listed

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