Ease-it Spray for the Treatment of Fire Ant Stings
Sponsor
C.R.Darnall Army Medical Center (U.S. Fed)
Overall Status
Completed
CT.gov ID
NCT00435552
Collaborator
(none)
Study Details
Study Description
Brief Summary
The application of Ease-it Spray will alleviate pain secondary to fire ant stings more quickly than placebo.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 1 |
Study Design
Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
Double
Primary Purpose:
Treatment
Study Start Date
:
Feb 1, 2007
Outcome Measures
Primary Outcome Measures
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
to 60 Years
Sexes Eligible for Study:
All
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
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- C.R.Darnall Army Medical Center
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
,
,
ClinicalTrials.gov Identifier:
NCT00435552
Other Study ID Numbers:
- C.2007.001
First Posted:
Feb 15, 2007
Last Update Posted:
Feb 15, 2007
Last Verified:
Jan 1, 2007