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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04250532
Other study ID # CHUBX 2019/48
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 26, 2020
Est. completion date July 15, 2020

Study information

Verified date June 2021
Source University Hospital, Bordeaux
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Drowning is the 3rd leading cause of accidental death in the world. One of the tools used by lifeguards to help ER assess gravity, is pulse oximetry. Its measure is variable even in optimal condition and its accuracy can be altered by factors specific to the patient and by environmental factors. The conditions gathered during a drowning rescue are thus propitious to a misleading evaluation. Assessing its reliability and looking for influencing factors of the measure of pulse oximetry could help for pre-hospital care management.


Description:

The research focuses on the measurement of pulse oximetry among lifeguard on the Atlantic coast of Gironde, France, before and after their daily training, using a standardized measurement protocol. The follow-up will be done during the beach monitoring period during the summer of 2020. A total of 3 months of measurement collection is expected.


Recruitment information / eligibility

Status Completed
Enrollment 31
Est. completion date July 15, 2020
Est. primary completion date July 15, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Lifeguard working on the Girondine Atlantic coast - up to 18 years old, - no smoker, - No chronic pathology. Exclusion Criteria: - Chronic cardiac pathology, - Chronic respiratory pathology, - Acrosyndrome, - Smoker.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Drowning
Measurement of pulse oximetry, after lifeguard immersion during their morning training

Locations

Country Name City State
France Hopital Pellegrin Bordeaux

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Bordeaux

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Proportion of abnormal pulse oximetry measure Quantify the number of subjects, whose pulse oximetry is measured as abnormal (superior to 94%) after immersion for 15 min in the ocean, in real condition. 3 months after inclusion day
Secondary Variation of pulse oximetry according to individuals factors Measures of immersion time, BMI before / after immersion. 3 months after inclusion day
Secondary Variation of pulse oximetry according to environnementals factors Measures of air, water temperatures, felt air temperature, wet thermometer temperature, wind speed before / after immersion. 3 months after inclusion day
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