Este estudio se centra en comparar dos tratamientos para las infestaciones de piojos de la cabeza: la Lotion Verde Elimax con Emogreen y el Champú Antipiojos de Walgreens. Los piojos de la cabeza son un problema común que afecta a personas de todas las edades, especialmente a los niños. El estudio tiene como objetivo determinar cuál producto es más efectivo y seguro para tratar los piojos de la cabeza. La Lotion Verde Elimax actúa asfixiando y deshidratando físicamente los piojos y sus huevos a través de sus ingredientes, que incluyen un bio-alcano y cera de abeja. Esta investigación es importante porque podría proporcionar una solución más efectiva para quienes sufren de piojos de la cabeza, mejorando el confort y reduciendo el tiempo dedicado al tratamiento de las infestaciones. Los participantes en este estudio deben tener seis meses de edad o más y tener un caso confirmado de piojos de la cabeza. El estudio seguirá las directrices para ensayos clínicos de dispositivos médicos según las regulaciones de EE. UU. Los participantes utilizarán el producto según las instrucciones, lo que generalmente implica aplicar el tratamiento y usar un peine para piojos. Los investigadores supervisarán la seguridad verificando cualquier irritación en la piel o los ojos y otros eventos adversos. El objetivo es asegurar que el producto no solo funcione de manera efectiva, sino que también sea seguro para los usuarios. Al comparar los resultados de estos dos tratamientos, el estudio busca ofrecer una mejor orientación para las personas que lidian con los piojos de la cabeza.
Inclusion Criteria: * Gender: male / female. * Female subjects with childbearing potential who test negative for pregnancy and agree to use a reliable method of birth control (as described in section7.8) or remain * Age ≥ 6 months of age at the time of enrollment. * Subject must have an active head lice infestation defined as at least 5 live lice (adults and/or nymphs) and 5 live nits based on magnified observations, present on the scalp and/or hair, as determined by a trained evaluator. * Subject is in good general health based on medical history. * Following application per designated product timeline shampoo hair using Johnson's baby shampoo (See figure 4 for shampoo image) to rinse out the product according to the study product its IFU. Subject agrees not to additionally shampoo, wash, or rinse their hair or scalp for 24-hours post treatment. * The subject agrees not to cut or chemically treat their hair while participating in the study. * Subject agrees to follow all study instructions, including attending all follow-up appointments. * Agree to not use any other anti-lice treatment or medicated hair grooming products for the duration of the study (through Day 10 visit). * The parent or legal guardian of a child must be willing to have other family members screened for head lice. If other household members are found to have head lice and are eligible, they must be either enrolled in the study OR receive the standard of care at the site and in the same manner as study participants. * Have a single place of residence or agree to remain at the current residence for the duration of the study. * 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. Subject or his/her parent/legal guardian must be capable of understanding and providing written informed consent. Exclusion Criteria: * Application of any form of head lice treatment, whether prescription or over-thecounter (OTC), or home remedy for 14 days prior to their screening visit (Visit * 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. * History of allergy or hypersensitivity to active ingredients, or constituents of the test products. * Subject with any visible skin/scalp condition at the treatment site which, in the opinion of the investigative personnel, will interfere with the evaluation of the test product. * Subjects with chronic scalp disorder. * Subject or his/her legal guardian who, in the opinion of the investigative personnel, do not understand the subject requirements for study participations and/or may be likely to exhibit poor compliance with the required visits. * Females who are pregnant or nursing. * Hair longer than waist length. * Subject suspected or known not to follow instructions * Previous participation in this study or participation in any other investigational trial within the preceding 14 days. * The subject is directly affiliated to the investigator site personnel and/or their immediate families. Immediate family is defined as a spouse, parent, child, or sibling, whether biological or legally adopted. * The subject is an Oystershell employee or is an employee of a third-party organizations involved in the study. * Exclude families with 4 or more household members. * People with dreadlocks or clip in hair that cannot be removed or a person who does not want to remove these. * Hair that is too difficult to work with, assessed by the study staff. * Families excluded where lice exist however family member declines enrollment in the study. * Subjects who are receiving, or are expected to receive, any antibiotic therapy during the study period will be excluded. * No more than one working subject per household may be excluded from evaluation if he is assessed as being lice by himself or caregiver. Only working male can be excluded from evaluation if individual is bald or hair no longer than half inch and deemed lice free by himself or another adult. * All household members of the subject, other than excluded male adult, must be screened for head lice by a licenced head lice professional. If additional household members are found to have head lice and meet the study criteria, they will be referred to LSRN Research and enrolled in study. If a household member declines enrollment, all family members will be excluded from the study.
están designados en este estudio
de ser asignado al grupo placebo