Comparing standard blood oxygen measures to a new device in humans under changing oxygen conditions

Phase 1

• Conditions: Stroke; Global Hypoxia; Cardiac Bypass Related Embolism; Global Ischemia; Neurological - Other neurological disorders; Stroke - Haemorrhagic; Stroke - Ischaemic; Cardiovascular - Other cardiovascular diseases

• Registration Number: ACTRN12620000691943
• Lead Sponsor: A/Prof. Shieak Tzeng

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-06-22
• Last Update Posted: 29 June 2020

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 4

Inclusion Criteria

18-50 years old
Generally healthy
Non-smoker
People with a BMI 18.5-30 kg m^-2

Exclusion Criteria

History of migraines
History of respiratory or cardiovascular disease or specific renal impairment.
Currently taking diuretics, antacids, proton pump inhibitors, or histamine blockers.
Smoking
Under 18 or over 50 years of age
History of stroke or other neurological conditions
Pregnancy
A contrast enhanced medical scan in the past week
There will also be a set of within-trial cessation criteria: a resting heart rate above 140 bpm, a peripheral O2 saturation below 70%, subject intolerance or request, sudden headache or nausea, or mental abnormalities as assessed by a clinician (i.e.: confusion, incoordination of motor skills).

Study & Design

• Study Type: Interventional
• Study Design: Not specified