Ivermectin
DrugTwo single doses of oral ivermectin 400 mcg/kg (Days 1 and 8) plus 2 single applications of placebo lotion
Other names: Stromectol®
NCT Number: NCT00819520
The purpose of this study is to compare 2 single doses of ivermectin as tablets with 2 single applications of malathion 0.5% lotion (Days 1 and 8) in clearing head lice, in patients who have recently used standard head lice treatments without success.
Looking for future studies?
Notify Me2 year and older
All sexes
Interventional
Phase 3
Hopital Avicenne, Bobigny, Paris, France
Head lice infestation occurs frequently, primarily in children 3 to 11 years of age. In recent years an increasing prevalence of lice infestation in schools, day care centres, and summer day camps is believed to be partly due to increasing lice resistance to currently available standard treatments for pediculosis (infestation with lice). There is a need for new effective backup treatments for this common condition of head lice infestation. This is a double-blind, randomized, parallel-group, study in several clinical centres comparing ivermectin as tablets to malathion 0.5% lotion in the treatment of head lice. All enrolled patients participate in the primary phase of the study up to the Day 15 evaluation. Patients who are still infested with lice at Day 15 (treatment failures) will enter an extension phase and be treated in a double-blind, fashion with the opposite treatment (ie ivermectin or malathion). The study hypothesis is that ivermectin will be more effective than malathion in clearing head lice infestation , as measured by the proportion of patients who are lice-free at Study Day 15.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Two single doses of oral ivermectin 400 mcg/kg (Days 1 and 8) plus 2 single applications of placebo lotion
Other names: Stromectol®
Two single applications of malathion 0.5% lotion (Days 1 and 8) plus 2 single doses of placebo tablets
Other names: Prioderm®
Time frame: Study Day 15
Time frame: Study Days 2, 8, 22, 29
Time frame: throughout duration of the study (+ 30 days for spontaneously reported SAEs)
Johnson & Johnson Consumer and Personal Products Worldwide
Industry
A Randomised, Double-Blind, Multicentre Study to Compare the Efficacy and Tolerability of Oral Ivermectin to Malathion 0.5% Lotion in the Treatment of Head Lice Infestation
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT05565820
Ectoparasitic Infestations, Head Lice
Miami, Florida, United States
View Trial DetailsNCT00244439
Ectoparasitic Infestations, Infections
Scottsdale, Arizona, United States
View Trial DetailsNCT02974088
Ectoparasitic Infestations, Head Lice
Cambridge, United Kingdom
View Trial DetailsNCT05643820
Ectoparasitic Infestations, Infections
Abbottabad, KPK, Pakistan
View Trial Details