Comparative Efficacy of Lipid Based Artificial Tears vs Aqueous Based Artificial Tears in Managing EDE
Launched by SUPERIOR UNIVERSITY · Mar 29, 2025
Trial Information
Current as of September 25, 2025
Active, not recruiting
Keywords
ClinConnect Summary
This clinical trial is looking at two types of artificial tears to see which one works better for people with Evaporative Dry Eye (EDE). The trial compares lipid-based artificial tears (called Recuro) and aqueous-based artificial tears (called Softeal) over a period of six weeks. It includes 60 adults, aged 18 to 55, who have been diagnosed with EDE and have experienced dry eye symptoms for at least 1 to 3 months. To be eligible, participants should have a score that shows they have mild to severe dry eye symptoms and a test result indicating their tears are not lasting long enough.
If you join this trial, you will be asked to use one of the two types of artificial tears as part of your treatment. It's important to know that you cannot use other eye medications or wear contact lenses during this study. The goal is to find out which type of artificial tear helps relieve symptoms better, which can ultimately improve comfort and quality of life for those dealing with dry eyes.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Adults (both genders) aged 18-55 years diagnosed with evaporative dry eye (EDE).
- • Willingness to adhere to the prescribed treatment regimen (lipid-based or aqueous-based artificial tears).
- • Include patients with a history of dry eye symptoms for at least 1-3 months.
- • Ocular Surface Disease Index (OSDI) score ≥13, indicating the presence of mild to severe dry eye symptoms.
- • Patients with tear break-up time (TBUT) \<10 seconds, indicating tear film instability.
- Exclusion Criteria:
- • Use of any topical ophthalmic medications (e.g., lubricants, anti-inflammatory drugs, or cyclosporine) for dry eye within the last 1 month.
- • Active ocular infection or inflammation (e.g., conjunctivitis, uveitis).
- • History of ocular surgery or trauma within the past 6 months.
- • Participants currently wearing contact lenses or those who have worn contact lenses in the past three months.
- • Systemic conditions known to impact ocular surface health, such as uncontrolled diabetes, autoimmune disorders, or Sjögren's syndrome.
About Superior University
Superior University is a leading academic institution dedicated to advancing healthcare through innovative research and clinical trials. With a commitment to excellence in education and patient care, the university fosters a collaborative environment that brings together multidisciplinary teams of researchers, clinicians, and students. Superior University is focused on exploring novel therapeutic approaches and improving patient outcomes, leveraging its state-of-the-art facilities and cutting-edge technology. The institution adheres to the highest ethical standards and regulatory guidelines, ensuring the integrity and impact of its clinical research initiatives.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Lahore, Punjab, Pakistan
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported