ADVANCED CLINIC P194 Facial Cleansing Wipes Study for Contact and Non-Contact Lens Wearers


ADVANCED CLINIC P194 Facial Cleansing Wipes Study for Contact and Non-Contact Lens Wearers
Posted  July 8, 2024

START DATE07/29/2024
QUALIFICATIONSMales and Females Ages: 18-75
TIME REQUIREMENT2 visits
COMPENSATION$60

Inclusion Criteria – A subject may be eligible for study participation if all of the following criteria are met:

  • Subject is female  or male  ages 18-75.
  • Subject is a contact lens wearer (approximately 50% of the study population) or a non-contact lens wearer (approximately 50% of the study population).
  • Subject has self-perceived sensitive eyes (approximately 50% of the study population) or has self-perceived non-sensitive eyes (approximately 50% of the study population).
  • Subject’s best corrected visual acuity is equal or better than 20/200 at the baseline evaluation.
  • Subject reports no subjective ophthalmic irritation at the baseline evaluation.
  • Subject exhibits baseline lacrimation, eyelid, contact lens, and corneal scores of 0. Subject may exhibit slight or mild [level 1 or 2] irritation of the palpebral and/or bulbar conjunctivae at the baseline evaluation. This latitude is permitted to allow for those subjects who normally exhibit slight or mild irritation as a result of their contact lens wear, and/or environmental and seasonal factors.
  • Subject agrees not to introduce any new cosmetic or toiletry products during the study.
  • Subject is dependable and able to follow directions as outlined in the protocol and anticipates being available for all study visits.
  • Subject is willing to participate in all study evaluations.
  • Subject is in generally good health and has a current Panelist Profile Form on file at CRL.

Exclusion Criteria – A subject is not eligible for study participation if any of the following criteria are met:

  • Female subject (if applicable) is pregnant, nursing, planning a pregnancy, or not using adequate birth control.
  • Subject has received treatment with sympathomimetics, antihistamines, vasoconstrictors, non-steroidal anti-inflammatory agents, and/or systemic or topical corticosteroids within one week prior to initiation of the study.
  • Subject has a history of acute or chronic dermatologic, ophthalmic, medical, and/or physical conditions which would, in the opinion of the Principal Investigator, preclude application of the test material and/or could influence the outcome of the study.
  • Subject is currently taking certain medications which, in the opinion of the Principal Investigator, may interfere with the study.
  • Subject has known allergies to skin or eye treatment products or cosmetics, toiletries, and/or topical drugs.
  • Subject has a history of skin cancer, ocular cancer, or is currently undergoing treatment for active cancer of any kind.
  • Subject has insulin-dependent diabetes.

Conflicting Studies: Any other studies for the Face & Eyes.

Study dates:

V1:         MON.    7/29 ( 20 Mins)
V2:        MON.    8/26 ( 20 Mins)

Appointment times:  7:30 AM – 3:45 PM

 




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