Efficacy of AirGLovE in Difficult Venous Access

NACompletedINTERVENTIONAL
Enrollment

34

Participants

Timeline

Start Date

March 29, 2019

Primary Completion Date

April 16, 2019

Study Completion Date

April 16, 2019

Conditions
Cancer
Interventions
DEVICE

Airglove (TM)

A sterile polythene-balloon was inflated around the forearm using the AirGloveTM to 38.5oC at setting number-3 for 3 minutes, then removed and the degree of venodilation assessed by ultrasound.

DEVICE

Warm-water Immersion

The upper limbs (to the level of mid-humerus) of participants were immersed in a container filled with a mix of cold-and warm tap-water to 38.5oC for 3 minutes in the WWI method. Arms were towel-dried, and the degree of venodilation was assessed by ultrasound

Trial Locations (1)

G4 0BA

Glasgow Calenonian University, Glasgow

All Listed Sponsors
lead

Glasgow Caledonian University

OTHER

NCT05127668 - Efficacy of AirGLovE in Difficult Venous Access | Biotech Hunter | Biotech Hunter