drugset / Trial / NCT00779987
Autologous Serum Efficacy Study in Patients With Severe Dry Eye
RandomizedCrossoverQuadruple-blindTreatment
Summary
The purpose of this study is to compare the reduction in symptomatology of patients with severe dry eye treated with autologous serum and conventional artificial tears.
Timeline
- Start
- 2008-10
- Primary completion
- 2008-12
- Completion
- 2008-12
Outcome
Met primary endpoint
paper Autologous serum treatment showed a statistically significant (p = 0.002) higher OSDI decrease (50%) versus conventional treatment (22%). PMID 22670856 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Autologous serum | Unknown | 20 % | Other |
| Subject | Systane | Other / unclassified | — | — |