Temperature on Evaporative Dry Eye

Sponsor
He Eye Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05720754
Collaborator
(none)
45
1
3
4
11.3

Study Details

Study Description

Brief Summary

Ocular surface temperature of a normal person is around 34.6 degree centigrade. After instilling the eye drop, depending on the temperature of the eye drop and the ocular surface, the ocular surface temperature will temporally increase or decrease sightly. Warm feeling will make blood vessels dilated and more blood will pass through to bring more blood flow out of our body to the heated area of the body and makes cells more permeable. Therefore, heating the ocular surface with heated eye mask after instilling artificial tears has the possibility to improve drug permeability on the ocular surface.

Condition or Disease Intervention/Treatment Phase
  • Drug: Diquafosol tetrasodium
  • Device: Heated eye mask
N/A

Detailed Description

Evaporative dry eye (EDE) is common and can lead to ocular pain, decreased visual quality, and reduced quality of life. 3% diquafosol (DQS) ophthalmic solution and heated eye mask (HEM) have been found to be beneficial in reducing signs and symptoms of dry eye. Warm compress therapy temperature of 40 °C to 45 °C have been typically advocated to melt the meibium causing obstruction at the orifices of the meibomian gland, eventually allowing increased lipid layer of the tear film. While in impact of heat on the ocular surface (OS) has not been extensively studied. Controlled and precise application of heat has the ability to create a cascade of events in the skin and thus aids in facilitating a faster movement of molecules into and across the skin. Possible mechanisms of enhancing drug permeation include on the ocular surface could be: (mechanisms may operate individually or concurrently):

  • increase in drug diffusivity in the vehicle and/or in the ocular surface

  • increase in partitioning and diffusion

  • alteration in the lipid structure

  • increased local blood flow Therefore, the purpose of this RCT is to assess the impact of instilling 3% DQS ophthalmic solution follow by HEM raising the OS temperature by 40 degrees centigrade for 10 minutes.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
45 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Care Provider, Investigator, Outcomes Assessor)
Masking Description:
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 three groups.
Primary Purpose:
Treatment
Official Title:
Safety and Efficacy of Heated Artificial Tears Under Practical Conditions
Anticipated Study Start Date :
Apr 2, 2023
Anticipated Primary Completion Date :
Jul 1, 2023
Anticipated Study Completion Date :
Aug 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: DQS+HEM

Participants in the DQS+ group used DQS 1 drop 3 times/per day with heated eye mask for 2 weeks

Drug: Diquafosol tetrasodium
3% Diquafosol tetrasodium eye drops will be used to assess its usefulness in dry eye signs and symptoms
Other Names:
  • Diquas
  • Device: Heated eye mask
    Heated eye mask will be used to assess its usefulness in dry eye signs and symptoms

    Active Comparator: DQS

    Participants in the DQS group used DQS 1 drop 3 times/per day for 2 weeks

    Drug: Diquafosol tetrasodium
    3% Diquafosol tetrasodium eye drops will be used to assess its usefulness in dry eye signs and symptoms
    Other Names:
  • Diquas
  • Active Comparator: HEM

    Participants in the HEM group used heated eye mask 3 times/per day for 2 weeks

    Device: Heated eye mask
    Heated eye mask will be used to assess its usefulness in dry eye signs and symptoms

    Outcome Measures

    Primary Outcome Measures

    1. Non-invasive tear break-up time (NIBUT) [Day-0 (baseline), day-7, and day-14]

      Non-invasive initial tear film breaking time will be assessed using the Keratograph 5M (Oculus, Germany) topographer. Three sequentially readings will be captured, and the median value will be included in the final analysis. The median value will be recorded. Changes at day-14 and day-28 will be compare with baseline measurements. Comparison between groups at baseline, day-14 and day-28 will also be examined.

    2. Ocular Surface Disease Index (OSDI) [Day-0 (baseline), day-7, and day-14]

      OSDI, which is a questionnaire consisting of 12 questions for evaluating the effects of dry eye syndrome on vision, ocular symptoms and any condition associated with DED. The patient will answer each question on a scale ranging from 0 to 4, with 0 indicating 'none of the time' and 4 indicating 'all of the time'. If a certain question is deemed irrelevant, it will be marked as 'not applicable (N/A)' and excluded from the analysis. The OSDI total score is calculated according to the following formula. The scale ranges from 0 to 100, with higher scores representing more severe cases of dry eye syndrome. Changes at day-14 and day-28 will be compare with baseline measurements. Comparison between groups at baseline, day-14 and day-28 will also be examined

    Secondary Outcome Measures

    1. Fluorescein and lissamine conjunctival and cornea staining (CFS) [Day-0 (baseline), day-7, and day-14]

      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. Changes at day-14 and day-28 will be compare with baseline measurements. Comparison between groups at baseline, day-14 and day-28 will also be examined.

    2. Meibomian gland function and secretion quality [Day-0 (baseline), day-7, and day-14]

      Meibum quality will be assessed under a slit-lamp: Five meibomian gland 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) Changes at day-14 and day-28 will be compare with baseline measurements. Comparison between groups at baseline, day-14 and day-28 will also be examined.

    3. Tear Film Lipid Layer Score (TFLL) [Day-0 (baseline), day-7, and day-14]

      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. Changes at day-14 and day-28 will be compare with baseline measurements. Comparison between groups at baseline, day-14 and day-28 will also be examined.

    4. Tear meniscus height (TMH) [Day-0 (baseline), day-7, and day-14]

      Non-invasive first tear film breakup time using the Keratograph 5M (Oculus, Germany) topographer will be measured three times consecutively and the median value was recorded. Changes at day-14 and day-28 will be compare with baseline measurements. Comparison between groups at baseline, day-14 and day-28 will also be examined.

    5. Conjunctival hyperemia (RS score) [Day-0 (baseline), day-7, and day-14]

      Conjunctival hyperemia (RS score) will be assessed by Keratograph image (Oculus, Germany) of 1156*873 pixels, redness score (RS) (accurate to 0.1 U) was displayed on the computer screen that ranged from 0.0 (normal) to 4.0 (severe). Changes at day-14 and day-28 will be compare with baseline measurements. Comparison between groups at baseline, day-14 and day-28 will also be examined.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 90 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Age ≥18 years

    • The presence of at most one symptom including burning, foreign body sensation, itching or eye fatigue for 3 months

    • OSDI score ≥ 13 and TBUT <5 s or NIBUT < 10s

    • Able and willing to comply with the treatment/follow-up schedule

    Exclusion Criteria:
    • A recent history (past 30 days) of topical ophthalmic medication use, including antibiotics, steroids, non-steroidal anti-inflammatory drugs, or required the chronic use of topical ophthalmic medications

    • Eyelids or intraocular tumors that should not put pressure

    • Active allergy or infection or inflammatory disease that may have prevented the subjects from completing the study at the ocular surface

    • Any structural change in lacrimal passage

    • Glaucoma

    • Diabetes or other systemic, dermatologic, or neurologic diseases that affect the health of ocular surface

    • Use of any systemic anti-inflammatory drugs or medication that may interfere with tear production, such as antianxiety, antidepressive, and antihistamine medications within 3 months

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 He Eye Hospital Shenyang Liaoning China 110034

    Sponsors and Collaborators

    • He Eye Hospital

    Investigators

    • Study Chair: Emmanuel Eric Pazo, MD, PhD, He Eye Hospital, Shenyang, China

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    He Eye Hospital
    ClinicalTrials.gov Identifier:
    NCT05720754
    Other Study ID Numbers:
    • EDEDQS2023
    First Posted:
    Feb 9, 2023
    Last Update Posted:
    Feb 9, 2023
    Last Verified:
    Feb 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by He Eye Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 9, 2023