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Not yet recruitingNCT07097922Updated Aug 1, 2025

Compare the Clinical Efficacy of 3% Diquafosol and 0.1% Hyaluronic Acid in Patients With Dry Eye After LASIK

An interventional study of 3% Diquafosol Sodium Eye Drops and 0.1% hyaluronic acid in Dry Eye, sponsored by He Eye Hospital. Not yet recruiting. Open to participants aged 18 Years to 40 Years. Per ClinicalTrials.gov, last updated 2025-08-01.

Sponsored by He Eye Hospital · Not applicable, Interventional, and Other

From the registry’s dates

  • Primary completion was expected by May 2026, 5 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
140
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
All
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Study summary

The prevalence of refractive ametropia is rising year by year. Refractive surgery has become the main approach for adults to correct refractive ametropia, and postoperative complications have aroused extensive attention from clinicians. Dry eye after refractive surgery is one of the postoperative complications, which is an important cause of affecting the postoperative visual quality and satisfaction of patients. It was reported that 3% diquafosol (DQS) and 0.1% hyaluronic acid (HA) can relieve dry eye symptoms. This study aims to compare the efficacy of 3% DQS and 0.1% HA in treating dry eye after LASIK

Read the detailed description

The development of corneal refractive surgery is rapid, but the complications are still inevitable; postoperative dry eye is one of them. Dry eye after refractive surgery will affect not only the patient's postoperative satisfaction but also the patient's postoperative visual quality, resulting in blurred vision, not lasting vision, and other problems. The occurrence of postoperative dry eye is mainly due to using anesthetics during operation; corneal nerve injury and cell apoptosis; changes in corneal curvature; postoperative medication, and so on. The patient's bad living habits may aggravate the degree of postoperative dry eye.

Diquafosol sodium is a P2Y2 receptor agonist. P2Y2 receptors are present on conjunctival and corneal epithelial cells, among others, on the ocular surface. When diquafosol sodium is used, it can activate P2Y2 receptors on these cells. This activation triggers the opening of intracellular signaling pathways that stimulate tear secretion. Normal tear secretion is important for corneal nerve repair because tears contain a variety of nutrients and growth factors. In the state of dry eye, the inflammatory factors on the ocular surface increase, and the stability of the tear film decreases. Diquafosol sodium can help to restore the stability of tear film by promoting tear secretion. A stable tear film reduces corneal nerve stimulation by inflammatory factors on the ocular surface. A large area of corneal nerves is injured during LASIK surgery, and no study has shown that diquafosol sodium has a role in nerve recovery after LASIK Hyaluronic acid (HA) lubricates, relieving dry eyes, astringent eyes, and eye fatigue. It can also flush and dilute inflammatory mediators on the ocular surface, reduce tear osmotic pressure, promote ocular surface epithelial healing, and promote ocular surface fibronectin secretion and deposition.

This study aims to compare the efficacy of 3% diquafosol and 0.1% hyaluronic acid in treating dry eye after LASIK. The observation of changes in corneal nerves and immune-inflammatory cells was added, aiming to observe the repair effect of diquafosol sodium on corneal nerves

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Conditions studied

  • Dry Eye

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03

In context

Dry Eye Syndromes

1,292 studies on the registry are indexed under Dry Eye Syndromes; 191 are open to participants now.

This study's planned enrollment of 140 is above the median of 60 across 1,077 interventional studies indexed under Dry Eye Syndromes.

Browse Dry Eye Syndromes studies →

Lead sponsor

He Eye Hospital is the lead sponsor of 31 studies on the registry; 15 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • History of LASIK surgery for more than six months
  • Confirmed dry eye: patients complained of one of the subjective symptoms of ocular dryness, foreign body sensation, burning sensation, fatigue, discomfort, redness of the eyes, and fluctuating visual acuity; as well as (a) OSDI questionnaire score of ≥13 and (b) non-invasive tear break-up time (NITBUT) of \<10 s or (c) ocular surface staining assessed in >5 corneal patches/greater than 9 conjunctival patches
  • Participants were able to co-operate with the use of eye drops as required, complete the examination, and return to the hospital within the specified time for follow-up examinations to complete the follow-up visit.

Exclusion criteria

Exclusion Criteria:

  • Suspected of having keratoconus, a definite diagnosis of keratoconus or another type of corneal dilatation disease.
  • There is active inflammation or symptoms of infection in the eye
  • There are serious lesions in the accessory structures of the eye, such as defects or deformations of the eyelids
  • Patients with Connective tissue diseases and Autoimmune disorders (e.g., SLE, RA)
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Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
140 participants (estimated)

Study arms

  • Experimental
    Study group

    dry eye patients after LASIK

    Drug: 3% Diquafosol Sodium Eye Drops

  • Other
    Control group

    dry eye patients after LASIK

    Drug: 0.1% hyaluronic acid

Interventions

  • Drug3% Diquafosol Sodium Eye Drops

    3% Diquafosol Sodium Eye Drops were instilled into the inferior conjunctival vault of both eyes

  • Drug0.1% hyaluronic acid

    0.1% sodium hyaluronate eye drops were instillation into the inferior conjunctival vault of both eyes

06

What researchers measure

Primary outcomes

  1. Non-invasive tear break-up time (NITBUT)

    The Keratograph 5M (Oculus, Germany) topographer will assess non-invasive tear breakup time. Three sequential readings will be captured, and the median value will be included in the final analysis. The median value will be recorded

    Time frame: Baseline, week 4, week 12 and week 24

Secondary outcomes

  1. Conjunctivocorneal staining (CS)

    Fluorescein and lissamine staining of the ocular surface will be divided into three zones comprising nasal conjunctival, corneal, and temporal conjunctival areas. The staining score ranged from 0 to 3 for each zone, yielding a total score of 0-9 for the ocular surface

    Time frame: Baseline, week 4, week 12 and week 24

  2. Tear film lipid layer (TFLL) score

    Tear film lipid layer interferometry will be assessed using DR-1 (Kowa, Nagoya, Japan). The results will be graded as follows: grade 1, somewhat gray color, uniform distribution; grade 2, somewhat gray color, nonuniform distribution; grade 3, a few colors, nonuniform distribution; grade 4, many colors, nonuniform distribution; grade 5, corneal surface partially exposed

    Time frame: Baseline, week 4, week 12 and week 24

  3. Corneal Sensitivity Score

    Corneal sensitivity score measured with a Cochet-Bonnet esthesiometer (in mm filament length); the measurements will be done 3 times at every assessment session, and the median value will be recorded.

    Time frame: Baseline, week 4, week 12 and week 24

  4. Tear meniscus height (TMH)

    Tear meniscus height using the Keratograph 5M (Oculus, Germany) topographer will be measured three times consecutively, and the median value will be recorded.

    Time frame: Baseline, week 4, week 12 and week 24

  5. Conjunctival hyperemia (RS score)

    Conjunctival hyperemia (RS score) will be assessed by a keratograph image (Oculus, Germany) of 1156 × 873 pixels, with a redness score (RS) ranging from 0.0 (normal) to 4.0 (severe).

    Time frame: Baseline, week 4, week 12 and week 24

  6. Meibomian quality

    Meibomian quality will be assessed under a slit-lamp; eight meibomian glands in the middle parts of the eyelid will be assessed using a scale of 0 to 3 for each gland (0 represented clear meibum; 1 represented cloudy meibum; 2 represented cloudy and granular meibum; and 3 represented thick, toothpaste-like consistency meibum).

    Time frame: Baseline, week 4, week 12 and week 24

  7. Meibomian gland expressibility

    Meibomian gland expression: five meibomian glands in the middle part were evaluated on a scale of 0-3: 0, all glandsexpressible; 1, 3-4 glands expressible; 2, 1-2 glands expressible; and 3, no glands expressible

    Time frame: Baseline, week 4, week 12 and week 24

  8. Corneal nerves and immune/inflammatory cell change

    HRT III RCM (Heidelberg Engineering GmbH, Germany) will be used to record corneal nerves and immune/ inflammatory cell change. It can accurately scan the cornea from the upper cortex to the inner cortex and other different depth levels and accurately judge the specific level and scope of the lesion. Three representative images of the subbasal nerve plexus and epithelial DCs will be selected for analysis for each eye, considering criteria such as a whole image in the same layer, best focus, and good contrast.

    Time frame: Baseline, week 4, week 12 and week 24

  9. OSDI

    The Ocular Surface Disease Index (OSDI) is a tool used to assess the degree to which ocular surface disease affects a patient's visual function and related symptoms. It is a subjective, patient-self-reported questionnaire.The questionnaire mainly covers three functions, and eye irritation symptoms. There are usually 12 questions, and the answer options for each question usually include "none," "mild," "moderate," and "severe," and the corresponding scores are 0, 1, 2, and 3. A range of 0-12 is classified as normal or mild symptoms. A range of 13-22 is classified as moderate symptoms. 23-36 is classified as severe symptoms.

    Time frame: Baseline, week 4, week 12 and week 24

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Study locations

No study locations are listed for this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 1, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07097922
Lead sponsor
He Eye Hospital
Responsible party
Sponsor
First posted
Aug 1, 2025
Start date
Aug 1, 2025 (estimated)
Primary completion
May 1, 2026 (estimated)
Completion
May 1, 2026 (estimated)
Last update
Aug 1, 2025

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jul 2025. You cannot join it, but the record below documents what was studied.

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