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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT03787212
Other study ID # CR-6281
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date December 6, 2018
Est. completion date January 28, 2019

Study information

Verified date January 2020
Source Johnson & Johnson Vision Care, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is a prospective, contralateral, single-site, single-visit unmasked evaluation of external and internal eyelid temperature after treatment with the MiBo ThermoFlo.


Recruitment information / eligibility

Status Terminated
Enrollment 4
Est. completion date January 28, 2019
Est. primary completion date January 28, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Potential subjects must satisfy all the following criteria to be enrolled in the study:

1. The subject must read, understand, and sign the STATEMENT OF INFORMED CONSENT and receive a fully executed copy of the form.

2. Appear able and willing to adhere to the instructions set forth in this clinical protocol.

3. Between 18 and 80 (inclusive) years of age at the time of screening.

4. Subjects must possess a functional/usable pair of spectacles and bring them to the visit (only if applicable - to the investigators discretion).

Exclusion Criteria:

- Potential subjects who meet any of the following criteria will be excluded from participating in the study:

1. Currently pregnant or breastfeeding.

2. Any systemic disease (e.g., Sjögren's Syndrome), allergies, infectious disease (e.g., hepatitis, tuberculosis), contagious immunosuppressive diseases (e.g., HIV), autoimmune disease (e.g. rheumatoid arthritis), or other diseases, by self-report, which are known to interfere with participation in the study.

3. Clinically significant (Grade 3 or 4 on the FDA classification scale) slit lamp findings (e.g. corneal edema, neovascularization or staining, tarsal abnormalities or bulbar injection).

4. Grade 3-4 Percentage of Partial Meibomian Glands on the Pult 5-point grading scale.

5. Any active Ocular Infection or Inflammation

6. Any history of eyelid surgery or abnormality

7. History of Metal Implants in the Eyelids

8. Any known hypersensitivity or allergic reaction to ultrasound coupling gel.

9. LASIK Surgery within 2 weeks of the Baseline Visit.

10. Participation in any contact lens or lens care product clinical trial within 14 days prior to study enrollment.

11. History of MiBo ThermoFlo or Lipiflow treatment Within the Last 6 months.

12. Employee or immediate family member of an employee of clinical site (e.g., Investigator, Coordinator, Technician).

Study Design


Related Conditions & MeSH terms


Intervention

Device:
MiBo ThermoFlo
Test Device
Bruder Mask
Control Device

Locations

Country Name City State
United States University of Houston, College of Optometry Houston Texas

Sponsors (1)

Lead Sponsor Collaborator
Johnson & Johnson Vision Care, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Posterior Eyelid Temperature (Palpebral Conjunctiva) Ocular surface temperature is usually 34.03±0.51ºC in the normal eye. The temperature required to melt obstructive secretions in the Meibomian glands ranges from 32- 35°C but the more severely obstructed glands present in MGD could require a temperature of >40°C, for effective treatment. there is an approximate 5°C difference in temperature between heat applied on the external eyelid surfaces and that reaches the inner surface of the lids, where the meibomian glands are located. This difference was due to both dissipation of heat while passing through the lid tissues and to constant movement of blood through vasculature wicking heat away from the lids. Therefore, achieving the desired temperature of 40°C at the palpebral conjunctiva requires a constant heat of at least 45°C be maintained on the outer lid surface, a temperature which could be both uncomfortable and risk causing thermal injury to the eyelid skin. 12-minutes post treatment
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