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Clinical Trials in Egypt / NCT07191847
Recruiting Phase 4

Assessment of CataClear, Tear Film Stability, Tear Volume, and Dry Eye Symptoms Using Stem Cells Fortified Eye Drops

NCT07191847 · tracked via the Priya Life Science Egypt tracker
Phase
Phase 4
Started
2025-04-22
Last updated
2025-09-25

Condition(s) studied

Dry EyeCataract

Investigational drug(s) / intervention(s)

eye drops

eye drops: apply 2 drops 3 times daily for 12 weeks

Study summary

Dry Eye Disease (DED) is a multifactorial condition that affects the ocular surface, leading to discomfort, tear film instability, and potential visual disturbances. Its global prevalence ranges between 5% and 50%, making it a significant cause of reduced quality of life and a growing burden on healthcare systems. Cataract, defined as a progressive opacification of the lens, remains the leading cause of preventable blindness worldwide, responsible for about 33% of all cases, affecting an estimated 94 million people. Its incidence increases with age and is influenced by factors such as ultraviolet exposure, diabetes, smoking, and genetic predisposition. Low- and middle-income countries (LMICs) face a disproportionately high burden due to limited access to surgical care. The economic impact of cataract is profound, including both direct costs (surgery, post-op care) and indirect costs (lost productivity, caregiver dependency), with global productivity losses estimated at $53 billion annually. Beyond economics, cataract significantly impairs quality of life, contributing to psychological distress, depression, loss of independence, and increased risk of cognitive decline. Addressing this burden requires integrated strategies that ensure equitable access to treatment, reduce financial barriers, and include psychosocial support. In parallel, emerging regenerative therapies such as stem cell-fortified eye drops offer new hope. These treatments, utilizing mesenchymal stem cells (MSCs), aim to restore ocular surface health in conditions like DED by reducing inflammation and enhancing tissue repair. The current study evaluates the efficacy of such drops in improving tear film stability, tear volume, and overall clinical symptoms using advanced diagnostic tools.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Adults aged 18-80 years. * Diagnosed with dry eye disease (based on clinical criteria such as OSDI scores and Schirmer test results). Exclusion Criteria: * Exclusion Criteria: * History of ocular surgery or trauma. * Other ocular diseases (e.g., glaucoma, keratitis). * Systemic conditions that may interfere with study outcomes (e.g., autoimmune diseases).

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
British center for regenerative medicine Giza Egypt Recruiting

More Ace Cells Lab Limited trials in Egypt

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07191847 on ClinicalTrials.gov ↗ ← All trials in Egypt