Clinical Trials Directory

Trials / Completed

CompletedNCT03322917

Ocular Surface Syndrome Post-lasik, Outcomes of Treatment With Platelet Rich Plasma

A Prospective Interventional Non-randomized and Non-comparative Series of Cases of Patiens Suffering Ocular Surface Syndrome Post-LASIK: Outcomes After the Treatment With Platelet Rich Plasma

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
80 (actual)
Sponsor
Vissum, Instituto Oftalmológico de Alicante · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

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).

Detailed 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.

Conditions

Interventions

TypeNameDescription
BIOLOGICALPRP autologousAutologous platelet rich plasma: 1 drop / 6 times a day during 6 weeks

Timeline

Start date
2008-07-01
Primary completion
2013-01-17
Completion
2013-01-17
First posted
2017-10-26
Last updated
2017-12-04

Source: ClinicalTrials.gov record NCT03322917. Inclusion in this directory is not an endorsement.