Effectiveness of "No More" Anti-lice Medical Device to Kill Lice and Lice Eggs
Clinical Trial of Anti-Lice Treatment Using the Medical Device "No More" Which is Designed to Kill Lice and Lice Eggs on the Head.
1 other identifier
interventional
50
1 country
1
Brief Summary
The purpose of this study is to determine effectiveness of an Anti-lice treatment using the medical device "No More" which is designed to kill lice and lice eggs on the head.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Oct 2015
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2015
CompletedFirst Submitted
Initial submission to the registry
October 6, 2015
CompletedFirst Posted
Study publicly available on registry
October 7, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2016
CompletedOctober 7, 2015
October 1, 2015
1 year
October 6, 2015
October 6, 2015
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
No live lice eggs and/or live lice
1 day from second visit
Interventions
use the "No More" medical device as anti lice treatment
Eligibility Criteria
You may qualify if:
- Patients that are suffering from lice and lice eggs that agree to refrain from any other treatment or salve designed for the treatment of lice and/or lice eggs throughout the course of the research study.
- Patients that orally and in writing express their agreement to participate in the study - Consent in writing will be provided by two parents; Oral consent will be provided by the participants themselves.
You may not qualify if:
- Pregnant or nursing women.
- Patients lacking the faculties for proper judgment.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Pharmayedalead
Study Sites (1)
Prof. Avner Shemer clinic
Netanya, 42150, Israel
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Ben Berger
Prof. Avner Shemer clinic
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 6, 2015
First Posted
October 7, 2015
Study Start
October 1, 2015
Primary Completion
October 1, 2016
Study Completion
December 1, 2016
Last Updated
October 7, 2015
Record last verified: 2015-10