ISRCTN45553737
Completed
Not Applicable
A randomised, controlled, assessor-blind, clinical trial to compare Liceko® with Nix® / Lyclear® 1% permethrin creme rinse in the treatment of head lice.
Panin S.R.L (Italy)0 sites44 target enrollmentMay 24, 2011
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Head louse infestation
- Sponsor
- Panin S.R.L (Italy)
- Enrollment
- 44
- Status
- Completed
- Last Updated
- 11 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Both males and females, 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 follow\-up visits by study team members over the 14 days following first treatment
Exclusion Criteria
- •1\. People with a known sensitivity to any of the ingredients in Liceko ® or Nix® / Lyclear® 1% permethrin creme rinse, pyrethroid insecticides, or plants related to dandelions or chrysanthemums.
- •2\. People with a secondary 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 co\-trimoxazole 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 one 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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