Clinical trial

A Single Center, Randomized, Controlled Trial Comparing the Clinical Efficacy of 3% Diquafosol Tetrasodium and 0.1 % Hyaluronic Acid 0.1% in Diabetic Patients With Dry Eye Disease

Name
DMDEDQS-2022-12
Description
Diquafosol ophthalmic solution (DQS) stimulates P2Y2 receptors on the ocular surface, which enhances mucin secretion from goblet cells. Therefore, tear film stability and hydration of the ocular surface can be achieved independent from lacrimal glands function. While it has been observed that 0.1 percent hyaluronate (HA) in artificial tears promotes corneal re-epithelium and improves corneal healing.This prospective, open label pilot study will include 60 eyes of 30 diabetic patients diagnosed with DED and will be randomly assigned to either DQS (n=30 eyes) or ATD group (n=30 eyes). Participants in the DQS group will receive 3% Diquafosol ophthalmic solution, while HA group will receive 0.1% Sodium hyaluronate artificial tears. The dosage for both drugs will be one drop, six times per day for 4 weeks. Tear film lipid layer (TFLL), non-invasive breakup time (NITBUT), corneoconjunctival staining score (CS), meibum gland (MG), conjunctival hyperemia (RS score), ocular surface disease index (OSDI) will be assessed and compared at baseline, day-14, and day-28.
Trial arms
Trial start
2023-11-01
Estimated PCD
2023-12-01
Trial end
2024-01-30
Status
Not yet recruiting
Treatment
3% Diquafosol tetrasodium
3% Diquafosol tetrasodium eye drops will be used to assess its usefulness in diabetic dry eye symptoms
Arms:
DQS group
Other names:
Diquas
0.1% hyaluronate
0.1% hyaluronate eye drops will be used to assess its usefulness in diabetic dry eye symptoms and compared to 3% Diquafosol tetrasodium eye drops.
Arms:
HA group
Other names:
Artificial tears
Size
202
Primary endpoint
Non-invasive tear break-up time
Day-0 (baseline), day-14 and day-28
Eligibility criteria
Inclusion Criteria: * Age ≥18 years * Clinical diagnosed and confirmed with type 2 diabetes for one year or more * Able and willing to comply with the treatment/follow-up schedule * Bilateral signs and symptoms of dry eye disease Exclusion Criteria: * Participants with systemic immune-mediated illnesses, such as secondary Sjögren's syndrome or graft-versus-host disease * Patients using topical medication(s) for the treatment of ocular disorders such as glaucoma or allergic conjunctivitis were excluded from the study. * Previous ocular surgery or trauma * 1-month history of blepharal and periorbital skin disease or allergies * Severe dry eyes with corneal epithelial defect * Limbic keratitis * Pterygium * Corneal neovascularization * Glaucoma * Breastfeeding * Rheumatic immune systemic diseases * Herpes zoster infection * Pregnant women * Allergic to fluorescein * Contact lens wearers
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['NA'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'interventionModelDescription': 'Prospective, randomised control trial.', 'primaryPurpose': 'SUPPORTIVE_CARE', 'maskingInfo': {'masking': 'TRIPLE', 'maskingDescription': 'Masked examiner for all clinical assessments will not involved in the data collection or group allocation procedure for this research. The investigator will not be aware of the two groups.', 'whoMasked': ['CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 202, 'type': 'ESTIMATED'}}
Updated at
2023-10-10

1 organization

2 products

1 indication

Organization
He Eye Hospital
Product
Diquafosol