A Phase 2 interventional study of 0.5% Ivermectin lotion and Vehicle in Pediculosis Capitis, sponsored by United Laboratories. Completed at 1 site in Philippines. Open to participants aged 3 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2018-03-07.
Sponsored by United Laboratories · Phase 2, Interventional, and Treatment
This is a randomized, double-blind, placebo-controlled clinical study evaluating the efficacy and safety of a single application of 0.5% ivermectin lotion in Filipino subjects with head lice.
43 studies on the registry are indexed under Lice Infestations; 4 are open to participants now.
This study's enrollment of 120 is above the median of 105 across 42 interventional studies indexed under Lice Infestations.
Browse Lice Infestations studies →United Laboratories is the lead sponsor of 4 studies on the registry; none are open to participants now.
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Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
A drug or device being studied in a clinical trial.
It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Investigational drug or device
A drug or device being studied in a clinical trial.
It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Drug: 0.5% Ivermectin lotion
Drug: Vehicle
The intervention is composed of a single application of the 0.5% ivermectin lotion.
The intervention is composed of a single application of the vehicle control.
Proportion of participants cured of head lice infestation from their assigned product on day 2, day 8 and day 15 after the first treatment.
Time frame: Day 2 to day 15 after product application
Plan to share: No
No publications or documents are linked to this record.
This study is completed, as verified in Mar 2018. You cannot join it, but the record below documents what was studied.
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United Laboratories