Clinical study of Descemet's Stripping Automated Endothelial Keratoplasty using new type cannula

Clinical study of Descemet's Stripping Automated Endothelial Keratoplasty using new type cannula - Clinical study of DSAEK using new type cannula

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000015817

Enrollment

300

Registered

2014-12-02

Start date

2012-09-27

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

Descemet&#39

s Stripping Automated Endothelial Keratoplasty using new type cannula

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Bullous keratopathy patients who are indicated for DSAEK in Osaka University Hospital 2) Aged 20 years old and over 3) Written informed consent

Exclusion criteria

Exclusion criteria: 1) Bullous keratopathy patients who are not indicated for DSAEK 2) Those who have been decided not appropriate for enrollment by the principal investigator 3) Patients without doing follow-up visits

Design outcomes

Primary

Measure	Time frame
survival of the graft after surgery	—

Secondary

Measure	Time frame
success in the graft insertion, visual acuity, corneal endothelial cell density, complication	—

Countries

Japan

Contacts

Public ContactTakeshi Soma

Osaka University Graduate School of Medicine Department of Ophthalmology

soma@ophthal.med.osaka-u.ac.jp06-6879-3456

Outcome results

None listed

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

Clinical study of Descemet&#39;s Stripping Automated Endothelial Keratoplasty using new type cannula