Ease-it Spray for the Treatment of Fire Ant Stings

This study has been completed.

Sponsor:

Information provided by:

C.R.Darnall Army Medical Center

ClinicalTrials.gov Identifier:

NCT00435552

First received: February 14, 2007

Last updated: NA

Last verified: January 2007

History: No changes posted

Tracking Information
First Received Date ^ICMJE	February 14, 2007
Last Updated Date	February 14, 2007
Start Date ^ICMJE	February 2007
Primary Completion Date	Not Provided
Current Primary Outcome Measures ^ICMJE	Not Provided
Original Primary Outcome Measures ^ICMJE	Not Provided
Change History	No Changes Posted
Current Secondary Outcome Measures ^ICMJE	Not Provided
Original Secondary Outcome Measures ^ICMJE	Not Provided
Current Other Outcome Measures ^ICMJE	Not Provided
Original Other Outcome Measures ^ICMJE	Not Provided

Descriptive Information
Brief Title ^ICMJE	Ease-it Spray for the Treatment of Fire Ant Stings
Official Title ^ICMJE	Not Provided
Brief Summary	The application of Ease-it Spray will alleviate pain secondary to fire ant stings more quickly than placebo.
Detailed Description	Not Provided
Study Type ^ICMJE	Interventional
Study Phase	Phase 1
Study Design ^ICMJE	Allocation: Randomized Intervention Model: Single Group Assignment Masking: Double-Blind Primary Purpose: Treatment
Condition ^ICMJE	Insect Bites and Stings
Intervention ^ICMJE	Procedure: Ease-It Spray
Study Arm (s)	Not Provided
Publications *	Not Provided
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.

Recruitment Information
Recruitment Status ^ICMJE	Completed
Enrollment ^ICMJE	Not Provided
Completion Date	Not Provided
Primary Completion Date	Not Provided
Eligibility Criteria ^ICMJE	Inclusion Criteria: AD soldier in US Army Ages 18-60 Volunteer Absence of serious medical condition Past allergic reactions Asthma History of (h/o) IFA sting Exclusion Criteria: Inability to provide informed consent Known h/o hymenoptera allergic reaction Allergy to any component of the treatments Inability to follow-up Active medical condition Pregnancy
Gender	Both
Ages	18 Years to 60 Years
Accepts Healthy Volunteers	Not Provided
Contacts ^ICMJE	Contact information is only displayed when the study is recruiting subjects
Location Countries ^ICMJE	Not Provided

Administrative Information
NCT Number ^ICMJE	NCT00435552
Other Study ID Numbers ^ICMJE	C.2007.001
Has Data Monitoring Committee	Not Provided
Responsible Party	Not Provided
Study Sponsor ^ICMJE	C.R.Darnall Army Medical Center
Collaborators ^ICMJE	Not Provided
Investigators ^ICMJE	Not Provided
Information Provided By	C.R.Darnall Army Medical Center
Verification Date	January 2007
^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP

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