New shampoo aims to stop head lice from coming back
NCT ID NCT07660354
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a new shampoo (X92001483) that works by physically trapping and removing head lice, comparing it to a standard medicated rinse (Nix Cream Rinse with 1% permethrin). The goal is to see if the new shampoo is safe, effective at killing lice, and can prevent reinfestation better than the standard treatment alone. About 98 people with head lice will be treated and followed for several weeks.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- X92001483 (medical device shampoo with physical mode of action)
- What this could lead to
- If it works, this shampoo could offer a new way to prevent head lice reinfestation without relying on chemical insecticides.
- What could go wrong
- This is a small, early-stage trial with only 98 participants, so results may not apply to everyone. The product's preventive effect may not be better than existing treatments.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 98 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2026
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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1 year and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Gender: male / female. 2. 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. 3. Age ≥ 1 year of age at the time of enrollment. 4. 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). 5. 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. 6. The subject is in good general health based on medical history. 7. Female subjects of childbearing potential must have a negative pregnancy test at screening and agree to use a reliable method of birth control (as described in section 7.8) during duration of the study. 8. The parent or legal guardian of a child subject must consent to the screening of other household members for head lice. If additional household members are found to have head lice and meet eligibility criteria, they must be enrolled in the study for all household members to qualify for participation. 9. Have a single place of residence or agree to remain at the current residence for the duration of the study. 10. Subject agrees not to additionally shampoo, wash, or rinse their hair or scalp for 24-hours post treatment. 11. The subject agrees not to cut or chemically treat their hair while participating in the study. 12. Subject agrees to follow all study instructions, including attending all follow-up appointments. Exclusion Criteria: 1. 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). 2. Application of any topical medication of any kind on the hair or scalp for a period of 48 hours prior to the screening visit. 3. 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. 4. Known skin allergies, multiple drug allergies or multiple allergies to cosmetic products. 5. History of allergy or hypersensitivity to active ingredients, or constituents of the investigational or comparator products. 6. 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 investigational product. 7. Subjects with chronic scalp disorder. 8. 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. 9. Females who are pregnant or nursing. 10. Hair longer than waist length. 11. Subject suspected or known not to follow instructions 12. Previous participation in this study or participation in any other investigational trial within the preceding 14 days. 13. 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. 14. The subject is an Oystershell employee or is an employee of a third-party organization involved in the study. 15. People with dreadlocks or clips in hair that cannot be removed or a person who does not want to remove these. 16. Hair that is too difficult to work with as assessed by the study staff. 17. Families excluded where lice exist however a family member decline enrollment in the study. 18. Subjects who are receiving, or are expected to receive, any antibiotic therapy during the study period will be excluded. 19. No more than one working male subject per household may be excluded from evaluation if determined to be lice free by self-report or caregiver observation. 20. All household members of the subject, other than excluded male adult, must be screened for head lice by a certified 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.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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LSRN
RECRUITINGMaitland, Florida, 32751, United States
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