Tourniquets Type Combat Application Tourniquet: Proximal or Distal Location, Simple or Staggered on Upper and Lower Limb
NCT03218176 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30
Last updated 2017-11-01
Summary
A tourniquet is used to stop abundant bleeding when simple compression is not effective. The investigators will study the vascular suffering of the tourniquets according to their location on the limb: limb (arm / thigh) or distal (forearm / leg). Vascular suffering will be evaluated by the loss of the radial doppler flux for the tourniquets placed on the upper limb and in the tibial anterior to the lower limb by the loss of the pulse oximetry pulse and the collection of the signs described by the volunteers (pain, Paresthesia, cold sensation).
Conditions
Interventions
- DEVICE
-
Proximal single upper limb
Measurement of pain, pressure under tourniquet, feeling and abolition of pulse doppler and pulse oximetry
- DEVICE
-
Proximal staggered upper limb
Measurement of pain, pressure under tourniquet, feeling and abolition of pulse doppler and pulse oximetry
- DEVICE
-
Distal single upper limb
Measurement of pain, pressure under tourniquet, feeling and abolition of pulse doppler and pulse oximetry
- DEVICE
-
Distal staggered upper limb
Measurement of pain, pressure under tourniquet, feeling and abolition of pulse doppler and pulse oximetry
- DEVICE
-
Proximal single lower limb
Measurement of pain, pressure under tourniquet, feeling and abolition of pulse doppler and pulse oximetry
- DEVICE
-
Proximal staggered lower limb
Measurement of pain, pressure under tourniquet, feeling and abolition of pulse doppler and pulse oximetry
- DEVICE
-
Distal single lower limb
Measurement of pain, pressure under tourniquet, feeling and abolition of pulse doppler and pulse oximetry
- DEVICE
-
Distal staggered lower limb
Measurement of pain, pressure under tourniquet, feeling and abolition of pulse doppler and pulse oximetry
Sponsors & Collaborators
-
University Hospital, Brest
lead OTHER
Principal Investigators
-
Emilie Gelin, MD · CHU de Brest
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- OTHER
- Masking
- NONE
- Model
- CROSSOVER
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2017-07-31
- Primary Completion
- 2017-10-23
- Completion
- 2017-10-23
Countries
- France
Study Locations
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