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

No results posted yet for this study

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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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03218176 on ClinicalTrials.gov