the effect of Prokera slim in dry eye syndrome

the effect of Prokera slim in dry eye syndrome - the effect of Prokera slim in dry eye syndrome

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000022620

Enrollment

Registered

2016-06-07

Start date

2016-07-01

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

Dry eye syndrome

Interventions

Treatment by Prokera slim /

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Dry eye syndrome (DEWS score >=3)

Exclusion criteria

Exclusion criteria: 1. Diseases with potential corneal nerve injury 2. Ocular infection within 2 weeks 3. Ocular surgery within 3 months

Design outcomes

Primary

Measure	Time frame
Corneal dye staining score 5 days after treatment with Prokera slim	—

Secondary

Measure	Time frame
Visual acuity and ocular symptoms 5 days after treatment with Prokera slim	—

Countries

Japan

Contacts

Public ContactTetsuya Kawakita

Keio University School of Medicine Dept. of Ophthamology

kawakita@a2.keio.jp03-3353-1211

Outcome results

None listed

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