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Clinical Trial Summary

To evaluate the efficacy of autologous platelet-rich plasma eye drops (E-PRP) for the treatment of chronic ocular surface syndrome (OSS) following laser in situ keratomileusis (LASIK).


Clinical Trial Description

Prospective interventional consecutive case series including 156 eyes of 80 patients affected by chronic post-LASIK OSS who were treated with autologous E-PRP 6 times a day as monotherapy for 6 weeks. Assessment after treatment with E-PRP included: dry eye symptoms, change in corrected distance visual acuity (CDVA), corneal fluorescein staining (CFS) and conjunctival hyperemia. ;


Study Design


Related Conditions & MeSH terms

  • Dry Eye After LASIK-Laser in Situ Keratomileusis

NCT number NCT03322917
Study type Interventional
Source Vissum, Instituto Oftalmológico de Alicante
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Status Completed
Phase Phase 2
Start date July 1, 2008
Completion date January 17, 2013

See also
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