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Treatment of Dry Eye With Supplements

Treatment of Dry Eye With Supplements

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01364311
Enrollment
0
Registered
2011-06-02
Start date
2011-07-31
Completion date
2014-11-30
Last updated
2015-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dry Eye Syndromes

Keywords

Dry Eye Syndromes, Dietary Supplements, Vitamac® Tag and Nacht capsules, Lutein, Vitamin C, Zinc, ginkgo biloba, Flavinoids, Fishoil, Zeaxanthin, Vitamin E, Copper, Selen, Alpha Lipon acid, Break up time (BUT), Improvement of subjective symptoms of dry eye syndrome, Visual Acuity, Tear film osmolarity, OSI (Objective Scattering Index), Schirmer I test, Staining of the cornea with fluorescein, Impression cytology, Tear cytokines/chemokines, Data from patient diary how often Hylo-Comod® eye drops were used

Brief summary

Dry eye syndrome (DES) is a highly prevalent ocular condition inducing an inflammatory response on the ocular surface. Common symptoms include ocular discomfort, visual impairment and instability of the tear film with potential damage to the ocular surface. In addition, an intact tear film is important to provide a smooth optical surface, to act as a barrier to pathogens, to nourish the epithelial cells of the ocular surface and to prevent exsiccation. Alterations in the tear film composition, which can have their origin in several conditions, lead to tear film hyperosmolarity or instability resulting in DES. Regardless of the cause of DES, chronic dryness of the ocular surface leads to an increased susceptibility to oxidative stress, which is triggered by reactive oxygen species (ROS). This results in cell damage and activation of the immune system, keeping up inflammatory processes . In order to prevent ROS damage, several micronutrients such as vitamin C, E, and certain carotenoids, omega-3 free fatty acids, flavonoids and minerals have been used because of their antioxidant capacities. Based on this knowledge the potential of these antioxidant dietary supplements has been discussed as a treatment option for DES. Preliminary data support the hypothesis that antioxidant supplementations, in particular, supplementation with omega 3 fatty acids may be beneficial for patients with DES. The purpose of the present study is to test the hypothesis that treatment with dietary supplements improves subjective and objective symptoms of DES.

Interventions

DIETARY_SUPPLEMENTVitamac® Tag and Nacht capsules

Vitamac® Tag und Nacht Kapseln: Dosage 1 capsule Vitamac® Tag per day ingested in the morning, 1 capsule Vitamac® Nacht per day ingested in the evening. Vitamac® Tag: Lutein 12mg, Vitamin C 300mg, Zinc 10mg, ginkgo biloba 10mg, Flavinoids 25mg, Fishoil 300mg, administered for 12 weeks Vitamac® Nacht: Zeaxanthin 5mg, Vitamin E 60mg, Copper 1mg, Selen 20µg, Ginkgo Biloba 10mg, Flavinoids 25mg, Alpha Lipon acid 150mg), administered for 12 weeks

Sponsors

Medical University of Vienna
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Men and women aged over 18 years * History of dry eye syndrome for at least 3 months * Tear Break Up Time (BUT) \< 10 seconds or Schirmer I test \< 7 mm * At least 2 symptoms of dry eye syndrome (foreign body sensation, burning, photophobia, blurred vision, pain, itching) * -Normal ophthalmic findings except dry eye syndrome

Exclusion criteria

* Participation in a clinical trial in the 3 weeks preceding the study * Symptoms of a clinically relevant illness in the 3 weeks before the first study day * Presence or history of a severe medical condition that will interfere with the study aim as judged by the clinical investigator * Wearing of contact lenses * Intake of dietary supplements in the 3 months preceding the study * Glaucoma * Treatment with corticosteroids in the 4 weeks preceding the study * Topical treatment with any ophthalmic drug except topical lubricants in the 4 weeks preceding the study * Ocular infection or inflammation * Ocular surgery in the 3 months preceding the study * Sjögren's syndrome * Stevens-Johnson syndrome * Pregnancy, planned pregnancy or lactating

Design outcomes

Primary

MeasureTime frame
Improvement of subjective symptoms of dry eye syndrome12 weeks
Break up time (BUT)12 weeks

Secondary

MeasureTime frame
OSI (Objective Scattering Index)12 weeks
Schirmer I test12 weeks
Staining of the cornea with fluorescein12 weeks
Visual Acuity12 weeks
Tear cytokines/chemokines12 weeks
Data from patient diary how often Hylo-Comod® eye drops were used12 weeks
Impression cytology12 weeks
Tear film osmolarity12 weeks

Countries

Austria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026