Maitland, FLNCT07660354Now EnrollingIRB Ready

Lice; Head Lice Clinical Trial in Maitland, FL

Access cutting-edge lice; head lice treatment through this clinical trial at a research site in Maitland. Study-provided care at no cost to qualified participants.

Sponsored by Oystershell NV

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Expert Care in Maitland

Access lice; head lice specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related lice; head lice treatment provided free

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Check if you qualify for this lice; head lice clinical trial in Maitland, FL

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Maitland

    Convenient for FL residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Maitland site if eligible
  4. 4Begin participation

About This Lice; Head Lice Study in Maitland

To compare the safety, effectiveness, and preventive benefits of a medical device (X92001483) against Nix Cream Rinse (1% Permethrin) in people with head lice

Sponsor: Oystershell NV

Who Can Participate

Inclusion Criteria

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).
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.
The subject is in good general health based on medical history.
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.
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.
Have a single place of residence or agree to remain at the current residence for the duration of the study.
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.

Exclusion Criteria

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.
History of allergy or hypersensitivity to active ingredients, or constituents of the investigational or comparator 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 investigational 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 organization involved in the study.
People with dreadlocks or clips in hair that cannot be removed or a person who does not want to remove these.
Hair that is too difficult to work with as assessed by the study staff.
Families excluded where lice exist however a family member decline 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 male subject per household may be excluded from evaluation if determined to be lice free by self-report or caregiver observation.
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.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Maitland?

Yes, this clinical trial (NCT07660354) has an active research site in Maitland, FL that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Lice; Head Lice Treatment Options in Maitland, FL

If you're searching for lice; head lice treatment options in Maitland, FL, this clinical trial (NCT07660354) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Maitland research site is actively enrolling participants for this clinical trial. You'll receive care from experienced lice; head lice specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all lice; head lice clinical trials near you to find additional studies recruiting in your area.

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