EUCTR2011-001892-38-GB
Active, not recruiting
Not Applicable
A randomised, controlled, assessor-blind, clinical trial to compare Liceko ® with NIX/Lyclear 1% permethrin crème rinse in the treatment of head lice. - Is Liceko ® more effective than Lyclear against head lice?
Panin S.r.l.0 sites44 target enrollmentMay 19, 2011
DrugsLyclear creme rinse
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Panin S.r.l.
- Enrollment
- 44
- Status
- Active, not recruiting
- Last Updated
- 13 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Children and adults aged 6 months and over with no upper age limit. 2\. People who upon examination, are confirmed to have live head lice. 3\. People who give written informed consent, or if the participant is under 16 years of age whose parent/guardian gives written informed consent to participate in the study. 4\. People who will be available for home visits by MEC study team members over the 14 days following first treatment.
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range:
- •F.1\.2 Adults (18\-64 years) yes
- •F.1\.2\.1 Number of subjects for this age range
- •F.1\.3 Elderly (\>\=65 years) yes
- •F.1\.3\.1 Number of subjects for this age range
Exclusion Criteria
- •1\. People with a known sensitivity to any of the ingredients in Liceko spray or Lyclear 1% permethin creme rinse. 2\. People with a bacterial infection of the scalp (e.g. impetigo) or who have an active long term scalp condition (e.g. psoriasis of the scalp). 3\. People who have been treated with other head lice products within the previous two weeks. 4\. People who have bleached hair, or hair that has been permanently waved within the previous four weeks 5\. People who have been treated with the antibiotics CoTrimoxazole or Trimethoprim within the previous four weeks, or who are currently taking such a course. 6\. Pregnant or nursing mothers. 7\. People who have participated in another clinical study within 1 month before entry to this study. 8\. People who have already participated in this clinical study.
Outcomes
Primary Outcomes
Not specified
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