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Taking peopleEarly phase 1

Can Brief Exposure to Hyperoxia Improve Function After Chronic Spinal Cord Injury?

Key facts

Phase
Early phase 1

This trial has no sites in United States.

It has sites in one country. Choose a country to see its sites.

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 65 years old?

Source: NCT05467215, who can take part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
University of Alberta
Trial code
NCT05467215
Record updated
11 September 2026
Original description
This proof-of-principle study will determine if breathing an increased concentration of oxygen above the concentration in normal room air results in changes in the sensory and motor function in people with subacute or chronic, severe spinal cord injury (SCI).Read full original descriptionShow less

This proof-of-principle study will determine if breathing an increased concentration of oxygen above the concentration in normal room air results in changes in the sensory and motor function in people with subacute or chronic, severe spinal cord injury (SCI).

Inclusion: Individuals with traumatic SCI with onset ≥3 months prior,; Between 18 - 65 yr old,; ASIA Impairment Scale at discharge classified as A, B or C,; Injury level between C5 and T10,; Able to give informed, written consent.

Exclusion: Cardiac or cardiovascular disease,; Cancer,; Active urinary tract infection,; Signs of deep vein thrombosis in the legs,; Severe cognitive impairment,; Pulmonary dysfunction such as chronic obstructive pulmonary disease or acute respiratory infection,; Any condition which would be exacerbated by sitting or lying in one position for 2 hours, such as low back pain; Frequent uncontrolled autonomic dysreflexia,; Uncontrolled high blood pressure,; Active pressure sores,; Severe swelling of the feet and/or legs,; Pregnancy.

ClinicalTrials.gov NCT05467215