이 페이지는 자동 번역되었으며 번역의 정확성을 보장하지 않습니다. 참조하십시오 영문판 원본 텍스트의 경우.

Safety, Efficacy and Preventative Effect of a Head Lice Product (X92001483) vs. Nix Creme Rinse (1% Permethrin).

2026년 6월 16일 업데이트: Oystershell NV

In Vivo Testing : A Two-Arm, Randomized, Controlled, Investigator/Assessor-Blinded, Comparative Study to Evaluate the Safety, Efficacy, and Preventative Effect of a Head Lice Physically Acting Product: 2 in 1 SHAMPOO EU VERSION (X92001483) vs NIX CREME RINSE (1% Permethrin) in Subjects With Head Lice.

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

연구 개요

상태

모병

정황

개입 / 치료

상세 설명

Compare Safety, Efficacy and preventative effect of a medical device with a physical mode of action against Nix Cream Rinse (1% Permethrin) in Subjects with Head Lice in a two-arm, randomized, controlled, Investigator/Assessor-blinded comparative study.

연구 유형

중재적

등록 (추정된)

98

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

    • Florida
      • Maitland, Florida, 미국, 32751
        • 모병
        • LSRN

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 어린이
  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

설명

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.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 더블

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Medical Device X92001483
Treatment of subjects with head Lice with the standard of care product Nix Creme Rinse on day 0 and day 7, followed by intermediate application of the medical device (X92001483) with a physical mode of action applied every 3 days.
Treatment of subjects with Head Lice with a medical device (X92001483) with a physical mode of action on day 0, day 7, day 10, day 13 and day 14.
간섭 없음: Nix Cream Rinse (1% Permethrin)
Treatment of subjects with Head Lice with Nix Cream Rinse (1% Permethrin) with a physical mode of action on day 0 and day 7.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Preventative Effect
기간: 14 days
Determin whether subjects treated with the medical device X92001943 after treatment with Nix Creme Rinse maintain a higher cure rate at the end of the study compared with subjects treated only with Nix Creme Rinse.
14 days
Maintenance of cure rate over time
기간: day 3, day 7, day 10, day 13 and day 14
To assess the maintenance of cure over time: To compare cure rates between subjects treated with Nix Creme Rinse and the medical device X92001483 at interim visits in order to evaluate the presence and persistence of the preventive effect of the investigational product relative to standard of care product (Nix creme rinse) alone.
day 3, day 7, day 10, day 13 and day 14

2차 결과 측정

결과 측정
측정값 설명
기간
Time to re-infestation
기간: 14 days
Characterize the time to re-infestation in each treatment group
14 days
Number of live lice
기간: Day 0, day 3, day 7, day 10, days 13, day 14
To compare the number of live lice detected at each assessment across treatment groups.
Day 0, day 3, day 7, day 10, days 13, day 14
Local tolerability
기간: day 0, day 3, day 7, day 10, day 13 and day 14
To evaluate the local tolerability of the standard of care product and investigational product, as measured by subject reported symptoms (eg: burning, paraesthesia, pruritus) following application.
day 0, day 3, day 7, day 10, day 13 and day 14
Scalp and skin irritation
기간: day 0, day 3, day 4, day 7, day 10, day 13 and day 14
To evaluate scalp and skin irritation by study staff (secondary infection, erythema, excoriation) following product application.
day 0, day 3, day 4, day 7, day 10, day 13 and day 14
Adverse advents
기간: Day 0, day 3, day 7, day 10, day 13 and day 14
To record and characterize all treatment-emergent adverse events occurring during the study.
Day 0, day 3, day 7, day 10, day 13 and day 14

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

협력자

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2026년 5월 1일

기본 완료 (추정된)

2026년 9월 1일

연구 완료 (추정된)

2026년 12월 1일

연구 등록 날짜

최초 제출

2026년 6월 16일

QC 기준을 충족하는 최초 제출

2026년 6월 16일

처음 게시됨 (실제)

2026년 6월 22일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 6월 22일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 6월 16일

마지막으로 확인됨

2026년 6월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • OYS012-0025

개별 참가자 데이터(IPD) 계획

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아니요

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