Study of the TearCare System in Dry Eye Disease

NCT ID: NCT03588624

Last Updated: 2025-09-11

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 29 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-07-12
• Study Completion Date: 2018-11-08

Brief Summary

This study was conducted to evaluate the short-term (1 month) safety and effectiveness of a single TearCare procedure to treat adult patients with dry eye disease.

Detailed Description

This was a prospective, single-arm, post-market, exploratory treatment study designed to collect clinical data regarding the safety and effectiveness of the TearCare System. To reduce potential bias in the study, study staff performing the endpoint assessments was independent of the clinician performing the TearCare procedure.

In this study, all subjects received the TearCare procedure. The TearCare procedure included an in-office 15 minute treatment session with the TearCare System immediately (i.e. within 3 minutes) followed by manual expression of the meibomian glands using the Express Forceps. Subjects received one in-office TearCare procedure at the baseline visit and then had follow-up visits at 1 week and 1 month.

This study was conducted at 3 sites in the United States.

Conditions

Dry Eye

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

TearCare

All subjects in the study were successfully treated with the TearCare device and manual expression of their eyelids, one time at the baseline visit.

Group Type: EXPERIMENTAL

TearCare

Intervention Type: DEVICE

The TearCare procedure includes the delivery of thermal energy to the external surface of the eyelids for 15 minutes, immediately followed by manual expression of each eyelid.

Interventions

TearCare

The TearCare procedure includes the delivery of thermal energy to the external surface of the eyelids for 15 minutes, immediately followed by manual expression of each eyelid.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

1. At least 22 years of age

2. Reports dry eye symptoms within the past 3 months

3. Reports having to use artificial tears or lubricants regularly over the past month to relieve dry eye symptoms.

4. OSDI Score of ≥23

5. TBUT of ≤7 seconds in both eyes

6. Meibomian gland obstruction in both eyes based on a total Meibomian Gland Secretion Score ≤15 in each eye.

7. At least 15 glands in each lower eyelid should be expressible, with a sterile cotton swab, at the slit lamp.

8. Best spectacle corrected visual acuity of 20/100 or better in both eyes.

9. Willing and able to comply with the study procedures and follow-up

10. Willing and able to provide informed consent

11. English-speaking

Exclusion Criteria

1. Any active, clinically significant ocular or peri-ocular infection or inflammation

2. Recurrent clinically significant eye inflammation, other than dry eye, within 3 months prior to enrollment

3. History of eyelid, conjunctiva or corneal surgery (including refractive surgery) within the past year. In addition, subjects with any history of the following are excluded: chalazion surgery, surgery on the tarsal conjunctiva, radial keratotomy (RK), complicated blepharoplasty, lid reconstruction, or significant complications post-refractive surgery.

4. Any office-based dry eye treatment (e.g. IPL, thermal pulsation [Lipiflow], etc.) within 12 months prior to enrollment. In addition Blephex or debridement within 3 months prior to enrollment is an exclusion.

5. Meibomian gland expression within 6 months prior to enrollment. In addition, any history of meibomian gland probing is an exclusion.

6. In the clinical judgement of the investigator, meibomian glands have significant capping, atrophy, or are unable to be expressed, digitally or with a sterile cotton swab.

7. Contact lens use within the past 2 weeks (Subjects must refrain from wearing contact lenses for the duration of the study.)

8. Use of TrueTear device within the past 2 weeks (Subjects must refrain from using the TrueTear device for the duration of the study.)

9. History of Ocular Herpes Simplex or Ocular Herpes Zoster

10. Clinically significant ocular surface abnormalities that may affect tear film distribution or treatment (e.g. pterygium, anterior membrane dystrophy, etc.)

11. Clinically significant eyelid abnormalities in either eye (e.g. entropion/ectropion, blepharospasm, aponeurotic ptosis, lagophthalmos, notching of lid margin, distichiasis, trichiasis)

12. Clinically significant anterior blepharitis. In addition, collarettes or flakes of more than one quarter of the eyelid are excluded.

13. Clinically significant dermatologic or cutaneous disease of the eyelid or periocular area

14. Ocular trauma within 3 months prior to enrollment

15. Any active, clinically significant allergic, vernal, or giant papillary conjunctivitis

16. Known history of diminished or abnormal facial, periocular, ocular or corneal sensation

17. Corneal surface abnormalities such as corneal epithelial defects (other than punctate staining), ulcers, corneal epithelial dystrophies, keratoconus, and ectatic disease of the cornea

18. Punctal occlusion or punctal plug placement within 30 days prior to enrollment

19. Systemic diseases resulting in dry eye (e.g. autoimmune diseases such as Sjogren's syndrome, rheumatoid arthritis, lupus, Graves' disease, sarcoidosis, etc.)

20. Allergies to silicone tissue adhesives

21. Use of Restasis or Xiidra within 60 days prior to enrollment. Subject must also be willing to remain off these drugs for the duration of the study.

22. Use of antihistamines (oral or topical) within 10 days prior to enrollment. Subject must also be willing remain off antihistamines for the duration of the study.

23. Subject is currently on a systemic medication(s) (other than anti-histamines) that is known to cause ocular dryness (e.g. diuretics, anti-hypertensives, anti-depressants, hormone therapy) and whose dose of this medication(s) has not been stable within 30 days prior to enrollment. There must be no anticipated adjustments to the dose of these medications for the duration of the trial.

24. Subject has taken or is currently taking Accutane

25. Subject requires chronic use (i.e. for any portion of the study) of topical ophthalmic antibiotics, anti-glaucoma medications, steroids, non-steroidal anti-inflammatory medications or who has been on any of these medications within 30 days prior to enrollment

26. Subject is currently using Retin A or Latisse

27. Participation in another ophthalmic clinical trial within one year prior to enrollment. Subject must also be willing to refrain from another ophthalmic study for the duration of the study.

28. Co-existing condition, either ocular or non-ocular that, in the judgement of the investigator could affect the safety or effectiveness of treatment or the compliance of the subject to the protocol. Subjects who are pregnant or nursing or have active, wet macular degeneration are excluded.

• Minimum Eligible Age: 22 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Sight Sciences, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jaime C Dickerson, PhD

Role: STUDY_DIRECTOR

Sight Sciences

Locations

Eye Research Institute

Newport Beach, California, United States

Arlington Eye Physicians

Arlington Heights, Illinois, United States

Kentucky Eye Institute

Lexington, Kentucky, United States

Countries

United States

Provided Documents

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

06001

Identifier Type: -

Identifier Source: org_study_id