Title

Safety and Efficacy Study to Compare a 4% Dimethicone Foam and Nix Cream Rinse (1% Permethrin) in the Control of Head Lice
An Open Label Randomized Study to Compare the Safety and Efficacy of Silcap Plus (Approximately 4% Dimeticone) Against Nix Cream Rinse.
  • Phase

    N/A
  • Study Type

    Interventional
  • Status

    Completed No Results Posted
  • Study Participants

    31
The purpose of this study was to evaluate the efficacy of a dimethicone foam in the control of head lice and to compare the efficacy to a permethrin based product.
Study Started
Sep 30
2007
Primary Completion
Nov 30
2007
Study Completion
Nov 30
2007
Last Update
May 06
2008
Estimate

Other 4% dimethicone foam

The dimethicone foam is applied to dry hair and left on the hair for approximately 15 minutes. The product is then removed by washing the hair with baby shampoo. The foam is applied two time, separated by an interval of 7-9 days.

  • Other names: Oxykal, Neo-paraderma

Other 1% permethrin

Nix® Cream Rinse is applied as indicated on the product labeling. The cream rinse is applied to wet hair and left on the hair for 10 minutes. The hair is then rinsed with tepid water to remove the product, toweled dry, and combed with a detangling comb. The product is applied two times, separated by an interval of 7-9 days.

  • Other names: Nix cream rinse

1 Experimental

4% dimethicone foam

2 Active Comparator

1% permethrin

Criteria

Inclusion Criteria:

4 - 85 years of age
active head lice infestation of at least ≥ 10 live lice
short hair (hair no longer than 2 inches below the neck) or long hair (hair 2 inches below the neck to mid back)

Exclusion Criteria:

had received or used an investigational new drug within the 30 days immediately preceding the study
used any form of head lice treatment whether prescription, over-the-counter, or a home remedy for at least fourteen days prior to their study visit
used topical medication of any kind on the hair for a period of 48 hours prior to the visit
had a history of allergy to rag weed, permethrin, or mineral oil, or had taken trimethoprim or cotrimoxazole at evaluation or during the previous four weeks
Female subjects that were pregnant or breast feeding
No Results Posted