Research on efficacy and safety of the artificial cornea for bullous keratopathy

Research on clinical outcomes after implantation of artificial cornea. - Research on clinical outcomes after implantation of artificial cornea.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000051282

Enrollment

Registered

2023-06-07

Start date

2023-06-19

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

Implantation of artificial corneal endothelium

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients with corneal endothelial dysfunction who are resistant to repeated keratoplasty.

Exclusion criteria

Exclusion criteria: Patients with corneal endothelial dysfunction who has never had keratoplasty.

Design outcomes

Primary

Measure	Time frame
Subjective symptoms, visual acuity, intraocular pressure, anterior,and posterior segment optical coherence tomography(OCT),confocal	—

Countries

Japan

Contacts

Public ContactTakahiko Hayashi

Kikuna Yuda Eye Clinic Ophthalmology

takamed@gmail.com+81454353755

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026