A Post-Market Evaluation of LipiFlow Treatment in Cataract Surgery Practice

Johnson & Johnson (J&J)

Status: Completed

Conditions: Meibomian Gland Dysfunction (MGD); Cataracts

Treatments: Device: LipiFlow Thermal Pulsation System

Study type: Interventional

Funder types: Industry

Identifiers

NCT03708367

DRYE-102-SELF

Details and patient eligibility

About

This is a post-market, prospective, randomized, multi-center, bilateral, open-label, cross-over, comparative clinical study. Study group will undergo preoperative LipiFlow treatment and Control group will not receive preoperative LipiFlow treatment. Three months postoperatively, both groups will be evaluated for clinical outcomes and the Control group will receive LipiFlow treatment as the cross-over group. The Control group will be evaluated at 4 months postoperative for clinical outcomes.

Enrollment: 117 patients

Sex: All

Ages: 22+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria (all criteria apply to each study eye):

• Minimum 22 years of age.
• Bilateral cataracts for which phacoemulsification extraction and implantation with Symfony IOLs have been planned.
• Evidence of Meibomian Gland Dysfunction (MGD) in both eyes based on assessment of meibomian glands of the lower eyelid
• None to moderate dry eye symptoms with questionnaire
• Clear intraocular media other than cataract in each eye.
• Availability, willingness, ability and sufficient cognitive awareness to comply with the study protocol including: randomization; examination procedures; completion of planned bilateral cataract surgeries; compliance with no use of other MGD or dry eye treatments.
• Ability to understand, read and write English to consent to study participation and complete study questionnaires.
• Willingness to sign informed consent and HIPAA authorization or equivalent documentation necessary to comply with applicable privacy laws pertaining to medical treatment in the governing country.

Exclusion Criteria (all criteria apply to each study eye):

• Any medical finding that would predictably result in a postoperative best corrected distance visual acuity worse than 20/30 in either eye.

• Use of systemic or ocular medications that, in the opinion of the investigator, may affect vision or impact pupil dilation or iris structure.

• Irregular corneal astigmatism.

• Any clinically-significant corneal pathology / abnormality other than regular corneal astigmatism.

• Any clinically-significant pupil abnormalities.

• Subjects with conditions associated with increased risk of zonular rupture.

• Unwillingness or inability to stop wearing contact lens at least two weeks prior to the baseline visit.

• Known ocular disease or pathology that, in the opinion of the investigator, may affect visual acuity or require surgical intervention during the study.

• Systemic disease condition that causes dry eye.

• Unwillingness or inability to abstain from the use of systemic medications known to cause dryness for the study duration. Subjects must have discontinued these medications for at least 1 month prior to Preoperative Visit.

• Unwillingness or inability to abstain from the use of systemic antihistamines.

• Unwillingness or inability to abstain from use of prescription medications for treatment of MGD or dry eye. Subject must have dicontinued using prescription medications for MGD or dry eye at least 1 month prior to baseline preoperative visit #1 measurements.

• Any of the following ocular (eye or eyelid) conditions in either eye within 3 months prior to the LipiFlow treatment visit:

  • Prior intraocular, oculoplastic, corneal or refractive surgery procedure (LASIK, LASEK, RK, PRK, etc.).
  • Ocular trauma.
  • Ocular Herpes simplex or Herpes zoster (eye or eyelid) infection.
  • History of recurrent ocular inflammation.
  • Punctal plug insertion or punctal occlusion.

• Any of the following active ocular (eye or eyelid) conditions in either eye at the baseline Preoperative Visit #1 measurements:

  • Ocular infection.
  • Ocular inflammation.
  • Moderate to severe (Grade 2-4) allergic, vernal or giant papillary conjunctivitis
  • Severe (Grade 3 or 4) inflammation of the eyelid.
  • Eyelid abnormalities that affect lid function.
  • Ocular surface abnormality that may compromise corneal integrity.

• Concurrent participation or participation within 30 days prior to study visit in any other clinical trial.

• Planned monovision correction.

• Patient is pregnant, plans to become pregnant, is lactating or has another condition associated with the fluctuation of hormones that could lead to refractive changes.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: None (Open label)

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117 participants in 2 patient groups

Study Group: LipiFlow Treatment at PreOp

Experimental group

Description:

Study subjects that meet all inclusion and exclusion criteria will be randomized to receive LipiFlow Thermal Pulsation System treatment at preoperative visit before bilateral implantation with commercially-available Symfony Intraocular Lens

Treatment:

Device: LipiFlow Thermal Pulsation System

Device: LipiFlow Thermal Pulsation System

Control Group

Other group

Description:

Study subjects that meet all inclusion and exclusion criteria will be randomized to not receive the LipiFlow Thermal Pulsation System treatment at a preoperative visit before bilaterally implanted with the commercially available Symfony Intraocular Lens. Control Group will receive LipiFlow treatment as cross-over group at 3 months postoperative visit.

Treatment:

Device: LipiFlow Thermal Pulsation System

Device: LipiFlow Thermal Pulsation System