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Cryopreserved amniotic corneal bandage with drug delivery

Research on safety and efficacy of cryopreserved amniotic corneal bandage with drug delivery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONB-17013950
Enrollment
Unknown
Registered
2017-12-15
Start date
2017-12-31
Completion date
Unknown
Last updated
2017-12-18

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

Conditions

dry eye

Interventions

moderate or severe dry eye patients wearing cryopreserved amniotic corneal bandage with drug delivery:wear cryopreserved amniotic corneal bandage with drug delivery

Sponsors

The 2nd Affiliated hospital, Zhejiang University, School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. sign the informed consent of this research voluntarily; 2. moderate or severe dry eye patients with Positive corneal fluorescein staining.

Exclusion criteria

Exclusion criteria: Meet any one of the following criterias will not have the qualification to participate in this research: 1. unable or unwilling to sign a letter of consent or do not follow the research procedure; 2. have serious systemic diseases, such as heart and brain diseases and psychosis.

Design outcomes

Primary

MeasureTime frame
OSDI scale;Conjunctival congestion index;FLS scores;Conjunctival lissamine green staining;BUT;eye sight;—

Countries

China

Contacts

Public ContactXiuming Jin

2nd Affiliated hospital, Zhejiang University, School of Medicine

lzyjxm@zju.edu.cn+86 13989455778

Outcome results

None listed

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