A prospective study of the outcomes of Descemet membrane endothelial keratoplasty (DMEK)

A prospective study of the outcomes of Descemet membrane endothelial keratoplasty (DMEK) - A prospective study of Descemet membrane endothelial keratoplasty (DMEK)

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000027586

Enrollment

100

Registered

2017-06-01

Start date

2014-08-01

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Bullous keratopathy

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Bullous keratopathy, Fuchs endothelial dystrophy, pseudo-exfoliation syndrome, birth injury, corneal endothelitis, eye with low corneal endothelial cell density, because of unknown factors

Exclusion criteria

Exclusion criteria: patient who dont agree with the research

Design outcomes

Primary

Measure	Time frame
Visual acuity(logMAR),Endothelial Cell Density(ECD), Central Corneal Thickness(CCT),High-order Abberattions(HOAs), and VFQ-25 were assessed preoperatively, and at1,3, 6 months, 1, 2, 3, 4, and 5 years postoperatively.	—

Secondary

Measure	Time frame
Central retinal thickness, Cystoid macula edema(CME), posteior synechia, iris abnormality, operative time, graft unfolding timewere assessed preoperatively, and at1,3, 6 months, 1, 2, 3, 4, and 5 years postoperatively.	—

Countries

Japan

Contacts

Public ContactTakahiko Hayashi

Medical Techno Department of Ophthalmology

takamed@gmail.com+817038502167

Outcome results