Supplementation With a Highly-Concentrated Docosahexaenoic Acid (DHA) Triglyceride in Patients With Keratoconus
Keratoconus
About this trial
This is an interventional treatment trial for Keratoconus
Eligibility Criteria
Inclusion Criteria: Diagnosis of keratoconus stages I to III according to the Amsler-Krumeich classification Non-contact lens wearers No history of previous corneal surgery Capacity to volunteer and willing and able to follow the study protocol Exclusion Criteria: Advanced keratoconus (stage IV of the Amsler-Krumeich classification Other ectasias (e.g. iatrogenic secondary to ocular surface surgery with excimer laser, radial keratotomy, traumatic corneal ectasia, etc.) Eyelid alterations Previous ocular surgery Any ocular or systemic condition that may affect the interpretation of results Glaucoma or ocular hypertension History of ocular trauma, infection or inflammation Current treatment with topical or anti-inflammatory drugs Use of nutritional supplements including omega-3 fatty acids, vitamins and minerals (unless a washout period of 1 month had been established) Hypersensitivity to fish proteins Pregnant women Refusal to sign the written informed consent
Sites / Locations
- FISABIO Medical Ophthalmology (FOM)
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
DHA group
Control group
Supplementation with a highly-concentrated docosahexaenoic acid (DHA) triglyceride (1000 g/day) for 3 months
Routine care