Efficacy and Safety of Topical 0.5% Ivermectin Lotion for the Treatment of Head Lice Infestation in Filipinos

NCT ID: NCT03286101

Last Updated: 2018-03-07

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 120 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-09-14
• Study Completion Date: 2017-11-09

Brief Summary

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.

Conditions

Pediculosis Capitis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

0.5% Ivermectin Lotion

Group Type: EXPERIMENTAL

0.5% Ivermectin lotion

Intervention Type: DRUG

The intervention is composed of a single application of the 0.5% ivermectin lotion.

Vehicle control

Group Type: PLACEBO_COMPARATOR

Vehicle

Intervention Type: DRUG

The intervention is composed of a single application of the vehicle control.

Interventions

0.5% Ivermectin lotion

The intervention is composed of a single application of the 0.5% ivermectin lotion.

Intervention Type: DRUG

Vehicle

The intervention is composed of a single application of the vehicle control.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Index subjects must have an active lice infestation defined as: At least 3 live lice (adult and/or nymphs) present on the scalp and/or hair as determined by a trained evaluator; After the index subject has been enrolled, additional infested household members will be enrolled.
• Household subjects must have an active head lice infestation defined as: At least 1 live louse (adult and /or nymph) present on the scalp and/or hair, as determined by a trained evaluator (with the exception of the male head of household who may self- assess, as being lice free).
• Subject is male or female;
• Subject is at least 3 years old or older at the time of enrollment;
• Subject is in good general health based on the medical history;
• Each adult subject must have an appropriately signed Informed Consent agreement. For children, parents/guardian must sign an Informed Parental Consent agreement for children not old enough to do so. Children of a specified age will be administered a child's assent form
• The caregiver of a subject must be willing to allow all household members to be screened for head lice. If other household members are found to have an active head lice infestation, they must be willing and able to participate in the study. No more than one working male per household maybe excluded from evaluation if he is assessed as being lice free by himself or the caregiver and cannot come in due to his work schedule. If this individual may have lice, he must come to the test facility, otherwise the entire household will be excluded from study participation.
• Subject and/or caregiver must be physically able and willing to report to the testing center for the supervised application of the product.
• Subjects agrees not to use any other form of lice treatment (commercial or mechanical/manual) while participating in the study;
• Following application and rinsing of the test product, subject agrees not to shampoo / wash, or rinse their hair or scalp until the 24-hour post treatment evaluation has been completed;
• Subject agrees to not cut or chemically treat their hair while participating in the study;
• Subject agrees to follow all study instructions.

Exclusion Criteria

• History of irritation or sensitivity to ivermectin or lotion components pediculosis or hair care products;
• Presence of visible skin / scalp conditions that are not attributable to head lice infestation, such as erythema, blisters, vesicles which in the opinion of the investigative personnel will interfere with safety and / or efficacy evaluations;
• Subjects suffering from psoriasis, atopic dermatitis or other conditions, which in the opinion of the investigator may compromise the objective of the study;
• Treatment for head lice (OTC, home remedy or Rx) in the last 14 days;
• Subjects under treatment which in the opinion of the investigator will interfere with the study results;
• Subjects who participated in a previous investigational drug study within the past 30 days;
• Subjects who does not understand the requirements for the study participation and/ or likely exhibit poor compliance, in the opinion of the investigator;
• Females who are pregnant or lactating.
• Living in a household where at least one member is pregnant, lactating, or planning a pregnancy
• Subjects with skin lesions, specifically skin breaks are excluded because of possible absorption of the drug

• Minimum Eligible Age: 3 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

United Laboratories

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Gertrude Chan, M.D.

Role: PRINCIPAL_INVESTIGATOR

Clinical Trial Management and Testing Associates, Inc.

Locations

Clinical Trial Management and Testing Associates, Inc.

City of Muntinlupa, , Philippines

Countries

Philippines

Other Identifiers

RD2017-01

Identifier Type: -

Identifier Source: org_study_id