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Taurine Eye Drops May Prevent the Progression of Cataract

Taurine Affects the Progression of Senile Cataract: a Single-arm Pre-post Intervention Study

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06639711
Enrollment
50
Registered
2024-10-15
Start date
2023-07-10
Completion date
2024-12-20
Last updated
2024-12-09

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

Conditions

Cataract

Brief summary

The aim of the current intervention study is to determine the effectiveness of taurine containing eye drops (available under brand name VIZILOTON) to prevent the progression of grade I and II senile cataract. This study could answer: * Dose continuous use of taurine-containing eye drops could prevent further deterioration of vision in mild cases of cataract? * The acceptance/ compliance of participants to taurine-containing eye drops. * Could long-term use of taurine-containing eye drops cause adverse effect(s)? Participants will: * Take taurine-containing eye drops (VIZILOTON eye drops) 4 times a day for one year. * Visit eye clinic every 3 months for assessment and visual examination. * Keep notes for their symptoms and their adherence to treatment.

Interventions

Taurine-containing eye drops (VIZILOTON) are applied 4 times daily for a period of one year

Sponsors

University Of Anbar
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

single-arm pre-post intervention study

Eligibility

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

Inclusion criteria

* The presence of grade I or II senile cataract on one or two eyes.

Exclusion criteria

* clinical signs of glaucoma * history of amblyopia, eye surgery, argon or YAG laser eye treatment, or major eye trauma * history of iritis, retinal crystalline deposits, or optic nerve disease * visually significant fundus pathology

Design outcomes

Primary

MeasureTime frame
Visual Acuity1 Year

Countries

Iraq

Outcome results

None listed

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