About this trial
To compare the safety, effectiveness, and preventive benefits of a medical device (X92001483) against Nix Cream Rinse (1% Permethrin) in people with head lice
Eligibility criteria
Qualifiers
Gender: male / female.
The subject or his/her parent/legal guardian (from age 12-17) must give written informed consent (after having been informed orally and by written text about the benefits and potential risks of the trial, as well as information regarding the insurance, taken out to cover the subjects participating in the study). A caregiver must sign an informed consent agreement for children not old enough to do so. Children aged 6-11 years of age will be administered a child's assent form. The subject or his/her parent/legal guardian must be capable of understanding and providing written informed consent.
Age ≥ 1 year of age at the time of enrollment.
Subject agree to not use any other anti-lice or preventative treatment or medicated hair grooming products for the duration of the study (through last visit day- Day 14).
Disqualifiers
Application of any form of head lice treatment, whether prescription or over-the counter (OTC), or home remedy for 14 days prior to their screening visit (Visit 1).
Application of any topical medication of any kind on the hair or scalp for a period of 48 hours prior to the screening visit.
Use of systemic or topical drugs or medications, including systemic antibiotics, which in the opinion of the investigative personnel may interfere with the study results.
Known skin allergies, multiple drug allergies or multiple allergies to cosmetic products.
Trial design
Treatments tested in this trial
- Medical Device (X92001483)
Treatment groups
Sponsors and collaborators
Oystershell NV
Lead sponsor
LSRN Research
Collaborator