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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00114894
Other study ID # 0311M54041
Secondary ID
Status Completed
Phase Phase 3
First received
Last updated
Start date April 2004
Est. completion date February 2006

Study information

Verified date April 2023
Source University of Minnesota
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Jellyfish stings are a common occurrence among ocean-goers worldwide with an estimated 150 million envenomations annually. Fatalities and hospitalizations occur annually, particularly in the Indo-Pacific regions. A new topical jellyfish sting inhibitor based on the mucous coating of the clown fish prevents 85% of jellyfish stings in laboratory settings. The field effectiveness is unknown. This is a field test to determine the real world effectiveness.


Description:

Jellyfish stings are a common occurrence among ocean-goers worldwide with an estimated 150 million envenomations annually. Fatalities and hospitalizations occur annually, particularly in the Indo-Pacific regions. A new topical jellyfish sting inhibitor based on the mucous coating of the clown fish prevents 85% of jellyfish stings in laboratory settings. Clown fish inhabit within the tentacles of sea anemones, which have stinging cells similar to those of jellyfish, yet clown fish are not stung by the sea anemones. In controlled laboratory environments, the jellyfish sting inhibitor, Safe Sea™ when applied to volunteers' arms, prevented 100% of Chrysaora fuscescens stings and 70% of Chiropsalmus quadrumanus stings. Of the C. quadrumanus stings that occurred, their intensity was diminished. The field effectiveness is unknown. This is a field test to determine the real world effectiveness of Safe Sea to prevent jellyfish stings.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date February 2006
Est. primary completion date January 2006
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Healthy volunteers planning on snorkeling for 30 to 45 minutes. Exclusion Criteria: - Pregnancy - Severe allergy to jellyfish - Allergy to any topical dermatologic product

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Safe Sea ™
Safe Sea ™ applied one time at 2 mg/cm2 coverage
Placebo
Placebo Coppertone® SPF15 sunscreen(Schering-Plough) applied at 2 mg/cm2 body coverage

Locations

Country Name City State
United States Dry Tortugas National Park Key West Florida

Sponsors (1)

Lead Sponsor Collaborator
Boulware, David R, MD

Country where clinical trial is conducted

United States, 

References & Publications (1)

Boulware DR. A randomized, controlled field trial for the prevention of jellyfish stings with a topical sting inhibitor. J Travel Med. 2006 May-Jun;13(3):166-71. doi: 10.1111/j.1708-8305.2006.00036.x. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of jellyfish stings during recreational saltwater exposure (~30 min)
Secondary Occurrence of seabather's eruption within 48 hours of saltwater exposure
Secondary impact of body hair on jellyfish stings after recreational saltwater exposure
See also
  Status Clinical Trial Phase
Recruiting NCT05394597 - Field Evaluation of Two Topically Applied Insect Repellent Products Containing IR3535 Against Mosquitos in Louisiana N/A