- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01685749
The Natural History of Human Stingray Injuries
Stingray injuries can be a hazard shared by many types of beachgoers. Stingrays often lie in the sand and when stepped on by the unsuspecting beachgoer their tail snaps foreword, resulting in a barbed stinger injecting venom into the victim. Little exists in the current literature on the natural history of stingray injuries. Most of the existing literature looks at the incidence of stings, and to a certain extent the demographic of people who seek care. To our knowledge no study has attempted to collect a more inclusive population of those people who are stung and follow them prospectively to determine the incidence of medical intervention, infection, etc.
This study aims to describe and quantify the natural history of stingray injuries and to better understand their time course and medical requirements. The study setting will be Seal Beach, which reports some of the greatest number of annual stingray injuries for any single beach on the pacific coast. Participants will be identified by the Seal Beach lifeguards who are believed to treat the majority of stingray injuries suffered at the beach. Eligible persons will be consented for participation over the phone by research personnel. If enrolled in the study they will receive a phone call by research personnel one week and one month after the injury that will collect information about the symptoms they have experienced and the medical interventions they have received, if any. This study is strictly observational in nature and will not involve any interventions on the part of study personnel or alter the manner in which or types of medical assessments or treatments.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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California
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Orange, California, United States, 92868
- University of California, Irvine Medical Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- People at Seal Beach, California
- People identified by Life guard personnel as being stung by a stingray at Seal Beach
- Adults or
- Children whose parent or guardian are present at the time of the injury
Exclusion Criteria:
- People who have previously been enrolled in the study
- People who the lifeguard believes were stung or bit by a marine organism other than a stingray or a terrestrial organism
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
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Enrolled participants
The targeted study population will include all people at Seal Beach who have been identified by the Seal Beach Lifeguards to have been stung by a jellyfish over the course of one year who are adults or children whose parent or guardian is present at the time of the injury.
Children and pregnant women are included in the group.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Incidence and duration of particular symptoms, medical evaluations, and treatment
Time Frame: up to 30 days from the date of injury
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This study is descriptive in nature.
The primary outcome of this study is the understanding of the natural history of stingray injuries and their treatment.
This will be achieved using strictly descriptive statistics of the incidence and duration of particular symptoms, medical evaluations, and treatment.
Means, proportions, and confidence intervals of these statistics will be calculated.
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up to 30 days from the date of injury
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HS#2011-8620
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Stingray Injury
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University of California, San FranciscoNational Center for Advancing Translational Sciences (NCATS)Not yet recruitingTrauma Injury | Survivorship | Injury TraumaticUnited States
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Oregon Health and Science UniversityCompletedInjury of Duodenum | Pancreatic InjuryUnited States
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