Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07583498

Spasticity in SCI Following Acute Intermittent Hypoxia

Led by Zev Rymer · Updated on 2026-05-13

10

Participants Needed

1

Research Sites

102 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to observe the effects of administration of a breathing intervention (Acute Intermittent Hypoxia (AIH)) on spasticity (tightness) in individuals with incomplete Spinal Cord Injury. It is hypothesized that hypoxia will decrease the reflex threshold of the biceps brachii, indicating an increase in spasticity following the AIH.

CONDITIONS

Official Title

Spasticity in SCI Following Acute Intermittent Hypoxia

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Non-progressive spinal cord injury at least 6 months prior
  • Injury level between C1 and C8
  • ISNCSCI ASIA classification C or D
  • Measurable spasticity
Not Eligible

You will not qualify if you...

  • Pre-existing hypoxic pulmonary disease
  • Positive Covid-Pneumonia diagnosis within 1 year
  • Uncontrolled hypertension over 140/90 mmHg
  • Currently pregnant, nursing, or planning pregnancy
  • Use of tracheostomy or mechanical ventilation
  • Botulinum toxin injection to upper extremity in past 3 months
  • Currently taking Baclofen
  • Congestive heart failure
  • Cardiac arrhythmias
  • Uncontrolled diabetes mellitus
  • Chronic obstructive pulmonary disease
  • Emphysema
  • Severe asthma
  • Previous myocardial infarction
  • Carotid or intracerebral artery stenosis
  • Orthopedic injuries or surgeries affecting upper extremity use
  • History of epilepsy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Shirley Ryan AbilityLab

Chicago, Illinois, United States, 60611

Actively Recruiting

Loading map...

Research Team

W

William Z Rymer, MD, PhD

CONTACT

A

Alexander Barry, MS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here