Ocular Surface Syndrome Post-lasik, Outcomes of Treatment With Platelet Rich Plasma
Launched by VISSUM, INSTITUTO OFTALMOLÓGICO DE ALICANTE · Oct 23, 2017
Trial Information
Current as of June 20, 2025
Completed
Keywords
ClinConnect Summary
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.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Adult patients suffering from moderate to severe dry eye syndrome for 6 months or more after conventional treatments with artificial tears following LASIK.
- • Tear break-up time (TBUT) between 4 and 9 seconds.
- Exclusion Criteria:
- • Ocular pathology needing topical treatments different than dry eye syndrome
- • Trombocitopeny, associated pathologies to coagulation factors or any state of plaquets antiagregation (AAS and other AINES).
- • Ocular tumours, corneal distrophies, history of ocular herpes.
- • Pregnant or nursering women.
About Vissum, Instituto Oftalmológico De Alicante
Vissum, Instituto Oftalmológico de Alicante, is a leading clinical research organization specializing in ophthalmology. With a commitment to advancing eye care through innovative research, Vissum conducts rigorous clinical trials aimed at evaluating cutting-edge treatments and technologies for a range of ocular conditions. The institute is equipped with state-of-the-art facilities and a team of experienced professionals dedicated to improving patient outcomes and contributing to the scientific community's understanding of vision-related health. Through collaboration with global partners, Vissum plays a pivotal role in shaping the future of ophthalmic therapies.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Patients applied
Trial Officials
JORGE L ALIO, DR.
Principal Investigator
Vissum, Instituto Oftalmológico de Alicante
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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