Resuscitation Clinical Trial
Official title:
Effects of Acute Hypobaric Hypoxia Exposure on Neurocognitive Performance of Pre-hospital Emergency Service Providers
The study aims to evaluate the effects of acute hypobaric hypoxia on cognitive performance
(H0: cognitive performance at 200 meters above sea level (asl) = cognitive performance at
3000 meters above sea level = cognitive performance at 5000 meters above sea level).
Before participating in the study, each participant will respond to a questionnaire related
to high altitude exposure (prior 3 months), as well as inclusion/exclusion criteria
evaluation.
On day 0, after the interview and signed informed consent, the participant will undergo a
medical examination that will include a general objective examination. Participants will
participate in a training on the emergency and safety procedures of the hypobaric hypoxia
facility, as well as a refresh on cardiopulmonary resuscitation procedure.
During the following two days (day 1 and 2) the study protocol will be executed (one test per
day). The study protocol envisages:
- a basal cognitive test battery
- blind ascent in the hypobaric chamber to simulated altitude
- cognitive test battery
- 5 minutes of recorded chest compressions on dummies
- cognitive test battery
- blind descent in the hypobaric chamber.
During the stay in the hypobaric hypoxic facility, each participant will be monitored in real
time with the Equivital© medical monitoring device.
Before and after the stay in the hypobaric hypoxic facility, a saliva sample will be
collected, and psychological tests administered.
n/a
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT04070560 -
Effects of Delayed Cord Clamping During Resuscitation of Newborn Near Term and Term Infants
|
N/A | |
Completed |
NCT03921346 -
Reducing Prehospital Medication Errors & Time to Drug Delivery by EMS During Simulated Pediatric CPR
|
N/A | |
Recruiting |
NCT04713358 -
Effect of Nalmefene on the Quality of Resuscitation in Patients Under General Anesthesia
|
Phase 4 | |
Recruiting |
NCT05029167 -
REstrictive Versus LIberal Oxygen Strategy and Its Effect on Pulmonary Hypertension After Out-of-hospital Cardiac Arrest (RELIEPH-study)
|
N/A | |
Completed |
NCT05474170 -
Impact of 2 Resuscitation Sequences on Management of Simulated Pediatric Cardiac Arrest
|
N/A | |
Completed |
NCT06070077 -
CPR Quality in Via Ferrata Rescues
|
||
Recruiting |
NCT03632837 -
HaemoAdsorption Nach Reanimation An ECMO
|
N/A | |
Completed |
NCT02575573 -
Resuscitation Decisions in the Emergency Department (ED)
|
N/A | |
Recruiting |
NCT02277405 -
Pediatric Intubation During Resuscitation
|
N/A | |
Completed |
NCT02277418 -
Venner a.p. Advance Video Laryngoscope
|
N/A | |
Terminated |
NCT00157989 -
Pilot Study to Assess Safety and Feasibility of Resuscitation of Preterm Infants With Controlled Volume of Air/Oxygen
|
Phase 3 | |
Completed |
NCT04500353 -
Routine Or Selective Application of a Face Mask for Preterm Infants at Birth: the ROSA Trial
|
N/A | |
Completed |
NCT01197807 -
Oronasopharyngeal Suction Versus Simple Nose and Mouth Wiping in Term Newborns
|
N/A | |
Completed |
NCT00719498 -
Effect of Early High-dose Epoetin Alfa During Cardiac Arrest (Pilot Study)
|
Phase 3 | |
Completed |
NCT04500197 -
A Study of MIcrocirculatory Perfusion Alterations in Severe Burn Injury
|
||
Recruiting |
NCT03345888 -
To Compare Predictive Power of End-tidal Carbon Dioxide Between Different Time Line During Resuscitation
|
N/A | |
Not yet recruiting |
NCT06376643 -
Augmented Reality to Support Cardiopulmonary Resuscitation
|
N/A | |
Completed |
NCT04034979 -
Evaluation of a Decision Aid About Life-sustaining Therapies
|
N/A | |
Recruiting |
NCT04699708 -
Co2 Monitoring at Preterm Delivery-Observational Study
|
||
Completed |
NCT05278884 -
Can VAST Improve ACLS in Rwanda
|
N/A |