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A prospective clinical study on the safety and efficacy of autologous plasma exosome therapy for dry eye syndrome

A prospective clinical study on the safety and efficacy of autologous plasma exosome therapy for dry eye syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115070
Enrollment
Unknown
Registered
2025-12-22
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Dry Eye Syndrome

Interventions

Experimental group:Autologous plasma exosome eye drop

Sponsors

Eye Hospital, Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Age range: 18 - 60 years old (inclusive). Gender is not restricted. 2. Patients with moderate to severe dry eye syndrome (in accordance with the Chinese Clinical Diagnosis and Treatment Expert Consensus on Dry Eye (2024)) who meet the diagnostic criteria, including corneal damage covering two quadrants or more, and/or corneal fluorescein staining point count >= 5, with TBUT below 5 seconds in both eyes. 3.Treatment history: Those who have not achieved satisfactory results or no effect at all from previous treatment plans for more than 3 months. 4. Voluntary participants who have signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Those who planned to undergo ocular surgery within 6 months prior to the screening period or during the study period. 2. Pregnant women or lactating women. 3. Having fungal, viral or bacterial keratitis or conjunctivitis, or other active inflammatory conditions of the ocular surface. 4. Wearing contact lenses. 5. Currently suffering from ocular herpes virus or any other eye infection or having a history of ocular herpes or any other eye infection within 30 days prior to the screening. 6. Eye and surrounding allergies, etc. 7. Other conditions deemed unsuitable for participating in the trial by the researchers.

Design outcomes

Primary

MeasureTime frame
Corneal fluorescein staining;

Countries

China

Contacts

Public ContactChi Zailong

Eye Hospital, Wenzhou Medical University

zailong.chi@eye.ac.cn+86 577 88075582

Outcome results

None listed

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