Efficacy and Safety of Summers Non-Pesticide Lice Asphyxiator (L.A.)for the Treatment of Head Lice.

Completed · Phase 3

Conditions studied: Head Lice

In brief

This is a multi-center, randomized, double blind, vehicle controlled, study designed to evaluate the pediculicidal activity of Summers 5% L.A. compared to a vehicle control.

Key facts

Study ID

NCT00301327

Run by

Summers Laboratories

People needed

120

Starts

2006-01-01

Last updated by the study team

2007-05-30

Who can join

Age: 1 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Males and females 6 months of age or older.
• Have an active infestation with pediculus capitis, the human head louse, with at least three live lice at baseline.
• Agree not to use any other pediculicides or medicated hair-grooming products during the duration of the study.
• Be healthy, non-febrile, and not suffering from an infection likely to require antibiotic therapy during the study period.
• Subject or guardian is able to understand the new HIPAA regulations and sign the HIPAA form.
• Subject or guardian has read, understood, and signed appropriate informed consent in English. If English is not the primary language, the information about the study must be explained in their language and a copy of the informed consent must be in that language.
• Subject is willing to participate in the study, and abide by the protocol requirements.

You may not qualify if…

• Participation in any clinical study within the past 30 days.
• Known hypersensitivity to any ingredient in the product formulation.

Where it is running

• Global Health Associates of Miami 7800, SW 57 Avenue, Suite 219E — Miami, Florida, United States
• Alegent Health, Harmony Street, 2nd Floor — Council Bluffs, Iowa, United States
• Dermatology Research Associates 7691 Five Mile Road, Suite 312 — Cincinnati, Ohio, United States
• Diagnostic Clinic of Longview, TX 707 Hollybrook Drive — Longview, Texas, United States
• Wee Care Pediatrics, 1580 West Antelope Drive, Suite 100 — Layton, Utah, United States

Full record on ClinicalTrials.gov

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