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Efficiency of a Jellyfish Sting Inhibitor Sun Lotion and Protocols for Jellyfish Sting Pain Relief

Efficiency of a Jellyfish Sting Inhibitor Sun Lotion and Protocols for Jellyfish Sting Pain Relief

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00693641
Enrollment
39
Registered
2008-06-09
Start date
2008-07-31
Completion date
2011-06-30
Last updated
2011-06-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain

Keywords

Jellyfish, Cyanea sp, Safe Sea, Prevention, treatment, Pain relief, Prevention of pain

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 effectiveness of hot/cold immersion for the treatment of Cyanea sp stings versus local pain relief with prescription free pharmaceutical drug (Xylocain 30 mg/ml (3%) lidocain).

Interventions

OTHERSafe Sea sun lotion with jellyfish sting protection SPF 15

Prevent or significantly reduce jellyfish sting using sun lotion with a jellyfish sting inhibitor. The amount of lotion applied to the skin before spreading is the same as for regular sun lotion 2.00 mg.cm-²± 2.5%.

OTHERNivea sun, caring sun lotion SPF 15

The amount of lotion applied to the skin before spreading is 2.00 mg.cm-²± 2.5%.

Sponsors

University of Oslo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Volunteers * men or women * aged 18 or over

Exclusion criteria

* 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.

Design outcomes

Primary

MeasureTime frameDescription
The purpose of the study is to investigate the effectiveness of a sun lotion containing a specific Jellyfish sting inhibitor versus regular sun lotions or no protection at all when in contact with Cyanea SP.Repeated jellyfish contact for total of 240 second or until pain occursWe want to find out how much longer it takes before you get stung if one at all gets stung when you have a protective layer on the skin. We also want to find out if the reduction in pain is significantly less when the skin has jellyfish protection using visual analog scale (VAS).

Secondary

MeasureTime frame
Investigate the effectiveness of hot/cold immersion for the treatment of Cyanea sp stings versus local pain relief with prescription free pharmaceutical drugs called Xylocain with lidocainePain relief treatment will start after 10 minutes, repeat treatment after 30 minutes if VAS score > 10.

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026