Status:
COMPLETED
Efficiency of a Jellyfish Sting Inhibitor Sun Lotion and Protocols for Jellyfish Sting Pain Relief
Lead Sponsor:
University of Oslo
Conditions:
Pain
Eligibility:
All Genders
18+ years
Phase:
PHASE4
Brief Summary
The purpose of the study is to investigate the effectiveness of a sun lotion containing a specific Jellyfish sting inhibitor versus regular sun lotions as controls. In addition, to investigate the eff...
Eligibility Criteria
Inclusion
- Volunteers
- men or women
- aged 18 or over
Exclusion
- People with atopic diseases, e.g., asthma, allergic rhinorrhea or rhinitis, hay fever, or atopic skin inflammation
- People who suffer from skin diseases in the testing regions or whose inner forearms are too hairy to allow for interpretation of the test
- People who have used any medical or cosmetic product on either arm for 48 hours before the start of the experiment
- People who are taking antihistamines or steroids
- Subjects with medical conditions which, in the opinion of the investigator, pose risks that would prohibit participating
- Subjects with a history of keloid formation will be excluded from the Jellyfish protocol
- Subjects with allergy to lidocain or other local pain substances
- If the arms contain hair that might reduce the jellyfish tentacle contact with the skin, the arm must be shaved in advance, so the skin has no sign of piling or any skin damage before the test.
Key Trial Info
Start Date :
July 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 1 2011
Estimated Enrollment :
39 Patients enrolled
Trial Details
Trial ID
NCT00693641
Start Date
July 1 2008
End Date
June 1 2011
Last Update
June 6 2011
Active Locations (1)
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1
University of Oslo, Biologisk Stasjon Drøbak
Biologveien 2, Drøbak, Norway, 1440