Head Louse Infestation, Pediculosis
Conditions
Brief summary
To assess the efficacy and safety of 10% Cocamide DEA using two treatment regimens in the eradication of head lice. To assess the ability of each treatment regimen to kill all viable ova and to assess patient acceptability of the product in use
Detailed description
A previous study found that a formulation of 10% cocamide diethanolamine (DEA) aqueous lotion showed some efficacy to eliminate head louse infestation but that the treatment regimen was inadequate to kill all lice or louse eggs. This study has been designed to compare two different application regimens that have been shown effective in vitro. A planned total of 120 patients who, following examination, are found to suffer from active head lice infestation will be recruited to the trial. The patient will be treated with 10% cocamide DEA lotion using the appropriate treatment regimen according to the randomization code from a pre-prepared listing in balanced blocks of 12. Group 1: 10% cocamide DEA is applied directly to dry hair, the excess water evaporated off using a hair dryer and is then left for 8 hour/overnight before washing off with clean water. Group 2: 10% cocamide DEA is applied directly to dry hair, the excess water evaporated off using a hair dryer and is then left for 2 hours before washing off with clean water. A follow up treatment is given after 7 days. Treatments will be applied by experienced investigators throughout the study. Assessments will be made by other investigators unaware of the treatment regimen used. After treatment (day 0), follow up assessments will be performed on days 4, 8,11 then again at day 14 after which they will leave the study. Any adverse events or side effects from the treatments will be monitored during the study.
Interventions
10% Cocamide DEA aqueous lotion is applied directly to dry hair and is washed off with water only
Sponsors
Riemann a/s
Medical Entomology Centre
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
4 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* Male and female patients over the age of 4 who are found to have a head louse infection. * Patients who give written informed consent and, if the patient is under 16 years of age, whose guardian gives written informed consent to participate in the study. * Available for the duration of study i.e. 15 days.
Exclusion criteria
* Patients with a known sensitivity to paraben preservatives. * Patients who have been treated with other head lice products within the last 2 weeks. * Patients who have undergone a course of antibiotic treatment within the last 4 weeks. * Patients who have any persistent skin disorder of the scalp (i.e. eczema, chronic dermatitis, psoriasis). * Patients whose hair has been bleached, colour treated or permed within the last 4 weeks. * Patients who have participated in another clinical trial within 1 month prior to entry to this study. * Patients who have already participated in this clinical trial.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Successful elimination of infestation | 14 days | No evidence of active head lice infestation 14 days after enrolment |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of participants with treatment related adverse events as a measure of safety | 14 days | No treatment related adverse events following treatment |
Outcome results
None listed