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Temperature on Evaporative Dry Eye

Primary Purpose

Dry Eye

Status
Not yet recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Diquafosol tetrasodium
Heated eye mask
Sponsored by
He Eye Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dry Eye focused on measuring dry eye, heated eye mask, diquafosol, tear breakup time, ocular surface disease index

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • He Eye Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Active Comparator

Arm Label

DQS+HEM

DQS

HEM

Arm Description

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

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

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

Outcomes

Primary Outcome Measures

Non-invasive tear break-up time (NIBUT)
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.
Ocular Surface Disease Index (OSDI)
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

Fluorescein and lissamine conjunctival and cornea staining (CFS)
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.
Meibomian gland function and secretion quality
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.
Tear Film Lipid Layer Score (TFLL)
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.
Tear meniscus height (TMH)
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.
Conjunctival hyperemia (RS score)
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.

Full Information

First Posted
January 31, 2023
Last Updated
January 31, 2023
Sponsor
He Eye Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05720754
Brief Title
Temperature on Evaporative Dry Eye
Official Title
Safety and Efficacy of Heated Artificial Tears Under Practical Conditions
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
April 2, 2023 (Anticipated)
Primary Completion Date
July 1, 2023 (Anticipated)
Study Completion Date
August 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
He Eye Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. 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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dry Eye
Keywords
dry eye, heated eye mask, diquafosol, tear breakup time, ocular surface disease index

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care ProviderInvestigatorOutcomes 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.
Allocation
Randomized
Enrollment
45 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
DQS+HEM
Arm Type
Experimental
Arm Description
Participants in the DQS+ group used DQS 1 drop 3 times/per day with heated eye mask for 2 weeks
Arm Title
DQS
Arm Type
Active Comparator
Arm Description
Participants in the DQS group used DQS 1 drop 3 times/per day for 2 weeks
Arm Title
HEM
Arm Type
Active Comparator
Arm Description
Participants in the HEM group used heated eye mask 3 times/per day for 2 weeks
Intervention Type
Drug
Intervention Name(s)
Diquafosol tetrasodium
Other Intervention Name(s)
Diquas
Intervention Description
3% Diquafosol tetrasodium eye drops will be used to assess its usefulness in dry eye signs and symptoms
Intervention Type
Device
Intervention Name(s)
Heated eye mask
Intervention Description
Heated eye mask will be used to assess its usefulness in dry eye signs and symptoms
Primary Outcome Measure Information:
Title
Non-invasive tear break-up time (NIBUT)
Description
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.
Time Frame
Day-0 (baseline), day-7, and day-14
Title
Ocular Surface Disease Index (OSDI)
Description
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
Time Frame
Day-0 (baseline), day-7, and day-14
Secondary Outcome Measure Information:
Title
Fluorescein and lissamine conjunctival and cornea staining (CFS)
Description
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.
Time Frame
Day-0 (baseline), day-7, and day-14
Title
Meibomian gland function and secretion quality
Description
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.
Time Frame
Day-0 (baseline), day-7, and day-14
Title
Tear Film Lipid Layer Score (TFLL)
Description
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.
Time Frame
Day-0 (baseline), day-7, and day-14
Title
Tear meniscus height (TMH)
Description
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.
Time Frame
Day-0 (baseline), day-7, and day-14
Title
Conjunctival hyperemia (RS score)
Description
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.
Time Frame
Day-0 (baseline), day-7, and day-14

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Emmanuel Eric Pazo, MD, PhD
Phone
0086-18612782131
Email
ericpazo@outlook.com
First Name & Middle Initial & Last Name or Official Title & Degree
Chen Jiayan, MSc
Phone
0086-18304019060
Email
chenjiayan@hsyk.com.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Emmanuel Eric Pazo, MD, PhD
Organizational Affiliation
He Eye Hospital, Shenyang, China
Official's Role
Study Chair
Facility Information:
Facility Name
He Eye Hospital
City
Shenyang
State/Province
Liaoning
ZIP/Postal Code
110034
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Emmanuel Eric Pazo, PhD
Phone
0086-18612782131
Email
ericpazo@outlook.com
First Name & Middle Initial & Last Name & Degree
Qin Guanghao, MD
Phone
0086-18842664420
Email
qinguanghao@hsyk.com.cn
First Name & Middle Initial & Last Name & Degree
Qin Guanghao, MD
First Name & Middle Initial & Last Name & Degree
Li Liangzhe, MD

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The study's findings will be shared regardless of the effect's direction. All possible beneficiaries of the research, including patients, carers, family, doctors, advisory boards, and medical boards, will receive trial data. Publications in high impact, open-access medical journals and talks at national and international medical conferences will serve this purpose.
IPD Sharing Time Frame
The Steering Committee will write and submit the report for publication at the end of the study
IPD Sharing Access Criteria
Use in clinical studies
Citations:
PubMed Identifier
32836200
Citation
Ma J, Pazo EE, Zou Z, Jin F. Prevalence of symptomatic dry eye in breast cancer patients undergoing systemic adjuvant treatment: A cross-sectional study. Breast. 2020 Oct;53:164-171. doi: 10.1016/j.breast.2020.07.009. Epub 2020 Aug 5.
Results Reference
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PubMed Identifier
28736340
Citation
Bron AJ, de Paiva CS, Chauhan SK, Bonini S, Gabison EE, Jain S, Knop E, Markoulli M, Ogawa Y, Perez V, Uchino Y, Yokoi N, Zoukhri D, Sullivan DA. TFOS DEWS II pathophysiology report. Ocul Surf. 2017 Jul;15(3):438-510. doi: 10.1016/j.jtos.2017.05.011. Epub 2017 Jul 20. Erratum In: Ocul Surf. 2019 Oct;17(4):842.
Results Reference
result
PubMed Identifier
17216085
Citation
Bron AJ, Tiffany JM. The contribution of meibomian disease to dry eye. Ocul Surf. 2004 Apr;2(2):149-65. doi: 10.1016/s1542-0124(12)70150-7.
Results Reference
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PubMed Identifier
29055358
Citation
Chhadva P, Goldhardt R, Galor A. Meibomian Gland Disease: The Role of Gland Dysfunction in Dry Eye Disease. Ophthalmology. 2017 Nov;124(11S):S20-S26. doi: 10.1016/j.ophtha.2017.05.031.
Results Reference
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PubMed Identifier
28736335
Citation
Craig JP, Nichols KK, Akpek EK, Caffery B, Dua HS, Joo CK, Liu Z, Nelson JD, Nichols JJ, Tsubota K, Stapleton F. TFOS DEWS II Definition and Classification Report. Ocul Surf. 2017 Jul;15(3):276-283. doi: 10.1016/j.jtos.2017.05.008. Epub 2017 Jul 20.
Results Reference
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PubMed Identifier
12649304
Citation
Kulkarni AA, Trousdale MD, Stevenson D, Gukasyan HJ, Shiue MH, Kim KJ, Read RW, Lee VH. Nucleotide-induced restoration of conjunctival chloride and fluid secretion in adenovirus type 5-infected pigmented rabbit eyes. J Pharmacol Exp Ther. 2003 Jun;305(3):1206-11. doi: 10.1124/jpet.103.049221. Epub 2003 Mar 20.
Results Reference
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PubMed Identifier
32280196
Citation
Dota A, Sakamoto A, Nagano T, Murakami T, Matsugi T. Effect of Diquafosol Ophthalmic Solution on Airflow-Induced Ocular Surface Disorder in Diabetic Rats. Clin Ophthalmol. 2020 Apr 1;14:1019-1024. doi: 10.2147/OPTH.S242764. eCollection 2020.
Results Reference
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PubMed Identifier
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Citation
Jumblatt JE, Jumblatt MM. Regulation of ocular mucin secretion by P2Y2 nucleotide receptors in rabbit and human conjunctiva. Exp Eye Res. 1998 Sep;67(3):341-6. doi: 10.1006/exer.1998.0520.
Results Reference
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PubMed Identifier
25179431
Citation
Tanioka H, Kuriki Y, Sakamoto A, Katsuta O, Kawazu K, Nakamura M. Expression of the P2Y(2) receptor on the rat ocular surface during a 1-year rearing period. Jpn J Ophthalmol. 2014 Nov;58(6):515-21. doi: 10.1007/s10384-014-0342-4. Epub 2014 Sep 2.
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PubMed Identifier
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Citation
Cowlen MS, Zhang VZ, Warnock L, Moyer CF, Peterson WM, Yerxa BR. Localization of ocular P2Y2 receptor gene expression by in situ hybridization. Exp Eye Res. 2003 Jul;77(1):77-84. doi: 10.1016/s0014-4835(03)00068-x.
Results Reference
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Temperature on Evaporative Dry Eye

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