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Savety and effectiveness evaluation of internal limiting membrane peeling with foveola nonpeeling in the treatment of myopic foveoschisis

Savety and effectiveness evaluation of internal limiting membrane peeling with foveola nonpeeling in the treatment of myopic foveoschisis

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900027668
Enrollment
Unknown
Registered
2019-11-23
Start date
2020-07-01
Completion date
Unknown
Last updated
2019-11-25

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:PPV combined with internal limiting membrane peeling with foveola nonpeeling

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 75 Years

Inclusion criteria

Inclusion criteria: 1) Dianosed with myopic foveoschisis usting fundus microscopy and optical coherence tomography; 2) Had refractive error of over -6.0 diopter; or axial length of over 26 mm; 3) Aged 18 to 75 years patient; 4) Patients are voluntarily involved in this clinical trial and signed informed consent

Exclusion criteria

Exclusion criteria: 1) combined with other vision-threatening eye diseases including macular hole, retinal detachment, choroidal neovascularization, glaucoma, etc; 2) Show improvment vision or self-healing tendency in the follow-ups; 3) combined with uncontrolled systemic disorders, such as hypertension,cardiovascular and cerebrovascular diseases, severe cardiac dysfunction, etc; 4) Had a history of ocular trauma, or a history of surgery in the affected eye; 5) Showed difficulties in cooperating with the operators.

Design outcomes

Primary

MeasureTime frame
Best corrected visual acuity;Central retinal thickness;the height of foveoschisis;

Countries

China

Contacts

Public ContactDezhi Zheng

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

zdz@jsiec.org+86 159 8984 9662

Outcome results

None listed

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