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The Effect of a Vapor Barrier in Combination With Active External Rewarming for Patients With Accidental Hypothermia

The Effect of a Vapor Barrier in Combination With Active External Rewarming for Patients

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05779722
Enrollment
16
Registered
2023-03-22
Start date
2023-03-08
Completion date
2024-03-15
Last updated
2023-03-22

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

Conditions

Hypothermia, Accidental

Brief summary

Most guidelines recommend the use of a vapor barrier when wrapping and isolating hypothermic patients from the environment, and this is especially important if the patient is wearing wet clothing. The vapor barrier will contain moisture evaporated from the wet clothes of the patient and increase the humidity. Once the humidity levels reach 100%, the evaporation and thereby the evaporative heat loss will stop. The theory is that the addition of a vapor barrier will reduce the amount of heat loss and contribute to more efficient rewarming of wet, hypothermic patients. We aim to investigate how much more efficient a wrapping model with active external rewarming is with the addition of a vapor barrier.

Detailed description

The study will use a crossover design on where research participants will undergo repetitions of the same scenario with different interventions in order to serve as their own control. The research participants will be healthy volunteers providing both oral and written consent. We intend to perform the experiments in an outdoor laboratory in order to achieve the most realistic conditions possible. The experiments will be conducted in Hemsedal, Norway in our Mountain Lab, a climate chamber built inside a snow cave. Before the start of the experiment, the research participants will be positioned in a supine position in the snow cave on an insulated stretcher in wet clothes saturated with a standardized amount of water.

Interventions

DEVICEVapor barrier

Vapor barrier

Sponsors

Haukeland University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

The study will use a crossover design on where research participants will undergo repetitions of the same scenario with different interventions in order to serve as their own control. We intend to perform the experiments in an outdoor laboratory in order to achieve the most realistic conditions possible. The experiments will be conducted in Hemsedal, Norway in our Mountain Lab, a climate chamber built inside a snow cave. Before the start of the experiment, the research participants will be positioned in a supine position in the snow cave on an insulated stretcher in wet clothes saturated with a standardized amount of water. They will stay in this position for 45 minutes to allow for a drop in the skin temperature without a drop in core body temperature. After 45 minutes, the research participant will be randomised into one of two scenarios, intervention or control.

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* healthy volunteers

Exclusion criteria

* any cronic sickness

Design outcomes

Primary

MeasureTime frame
Skin temperature45 minutes

Countries

Norway

Contacts

Primary ContactSigurd Mydske, PhD student
sigurd.mydske@norskluftambulanse.no+4790659586
Backup ContactØyvind Thomassen, PhD
oyvind.thomassen1@helse-bergen.no+4797718721

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026