Skip to content

Clinical observation of adhesive artificial endothelial layer for corneal endothelial dysfunction

Clinical observation of adhesive artificial endothelial layer for corneal endothelial dysfunction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072557
Enrollment
Unknown
Registered
2023-06-16
Start date
2023-06-16
Completion date
Unknown
Last updated
2023-06-18

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

Conditions

corneal endothelial dysfunction

Interventions

Experimental group:implantation of plasma treated artificial endothelium

Sponsors

Shandong Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) According to the current diagnostic criteria of corneal endothelial dysfunction, adult patients (over 18 years old) with corneal endothelial dysfunction were definitely diagnosed, regardless of gender; 2) Volunteer to participate in this observational study and sign the informed consent form; 3) Able to follow up for a long time in the hospital

Exclusion criteria

Exclusion criteria: 1) Patients with severe systemic diseases and contraindications to conventional clinical treatment; 2) There are any diseases in the body, and researchers think that the use of artificial corneal endothelium may make the subject face a greater risk; 3) Patients who cannot tolerate surgery; 4) Patients who cannot be followed up for a long time in the enrolled hospital.

Design outcomes

Primary

MeasureTime frame
Corneal thickness measurement;OCT examination of cornea;

Secondary

MeasureTime frame
confocal microscopy;Score of eye pain questionnaires;Endothelial specular microscopy ;

Countries

China

Contacts

Public ContactWeiyun Shi

Shandong Eye Hospital

weiyunshi@163.com+86 186 0531 0106

Outcome results

None listed

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