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corneal stromal lenticule implantation for hyperopia/ hyperopia after myopia correction/keratoconus

The application of stromal lenticules

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONh-17011978
Enrollment
Unknown
Registered
2017-07-13
Start date
2017-07-31
Completion date
Unknown
Last updated
2017-07-17

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

Conditions

hyperopia/hyperopia after myopia correction/keratoconus

Interventions

1:lenticule implantation

Sponsors

Fudan EENT Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Aged more than 18 years old and has the following any one situation: 1. hyperopia; 2. hyperopia after myopica correction; 3. keratoconous.

Exclusion criteria

Exclusion criteria: 1. current use of any medication due to a psychiatric disorder or cognitive impairment that might affect the psychological assessment; 2. subjects who had undergone ocular surgery within the last 6 months.

Design outcomes

Primary

MeasureTime frame
efficacy;safety;biomechanical changes;coneal structural changes;visual quality;wound healing process;—

Countries

China

Contacts

Public ContactXingtao Zhou

Fudan Eye & ENT Hospital

doctzhouxingtao@163.com+85 021 64377134

Outcome results

None listed

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