A Randomised, Controlled, Investigator-Blinded, Comparative Study to Evaluate the Safety and Efficacy of a Head Lice Shampoo - 02060024 in Head Lice

Oystershell Laboratories0 个研究点目标入组 109 人开始时间: 2015年12月7日最近更新: 2024年8月19日

适应症

试验速览

暂无简介。

•1. Gender: male/female
•2. Age: = 1 year of age at the time of signing the informed consent
•3. Patients with active head lice infestation of at least 5 live lice and 5 apparently live eggs
•4. Patient or his/her guardian must be capable of understanding and providing written informed consent
•5. The patient or his/her legal representative must give written informed consent, after having been oral and written informed about benefits and potential risks of the trial, as well as details of the insurance taken out to cover the subjects participating in the study
•6. Patients must agree to not use any other ant-lice treatment for the duration of the study
•7. Female patients: are women of childbearing potential who test negative for pregnancy and agree to use a reliable method of birth control or remain abstinent during the study. Methods of contraception considered acceptable include oral contraceptives, contraceptive patch, intrauterine device, vaginal ring, diaphragm with contraceptive gel, or condom with contraceptive gel
•are women of non–childbearing potential, defined as: women who have had surgical sterilization (hysterectomy, bilateral oophorectomy, or tubal ligation),
•women who are =60 years of age.

•1. Known allergic reactions or hypersensitivity to the active ingredients used or the constituents
•2. Patients with known skin allergies, multiple drug allergies or multiple allergies to cosmetic products
•3. Pregnant or breast feeding women
•4. Patient underwent treatment with any form of head lice treatment within the last 30 days prior to the Screening Visit (day 0)
•5. Patients with chronic scalp disorder
•6. Individuals on systemic or topical drugs or medications, including systemic antibiotics, which in the opinion of the investigative personnel may interfere with the study results
•7. Subjects with hair longer than mid-back
•8. Patients suspected or known not to follow instructions
•9. Patients or his/her legal representative who are unable to understand the written and verbal instructions, in particular regarding the risks and inconveniences they will be exposed to as a result of their participation in the study
•10. Previous participation in this study or participation in any other investigational trial within the preceding 30 days
•11. The patients are investigator site personnel directly affiliated with this study and/or their immediate families. Immediate family is defined as a spouse, parent, child, or sibling, whether biological or legally adopted
•12. The patients are Oystershell employees or are employees of third-party organizations involved in the study.

发起方

Oystershell Laboratories