← Back to Clinical Trials
Recruiting NCT07739992

NCT07739992 Dose Optimization Study of Acute Intermittent Hypoxia in Spinal Cord Injury

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT07739992
Status Recruiting
Phase —
Sponsor Milap Sandhu
Condition Spinal Cord Injuries (SCI)
Study Type INTERVENTIONAL
Enrollment 40 participants
Start Date 2026-07-27
Primary Completion 2027-07

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 75 Years
Study Type INTERVENTIONAL
Interventions
Sham AIHAcute Intermittent Hypoxia (AIH) 15Acute Intermittent Hypoxia (AIH) 23

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 40 participants in total. It began in 2026-07-27 with a primary completion date of 2027-07.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study aims to evaluate how different doses of acute intermittent hypoxia (AIH) affect lower-limb strength, reaction time, and responsiveness in individuals with spinal cord injury (SCI). The objective is to identify the dose that most effectively improves motor output while also examining parameters that may account for variability in response.

Eligibility Criteria

Inclusion Criteria: * Chronic Spinal Cord Injury (\>6 months) * Motor incomplete SCI classified as AIS C or D * Volitional ankle plantarflexion strength in at least one leg Exclusion Criteria: * Uncontrolled hypertension (outside 140/90 and 90/60) * Concurrent medical illness * Traumatic brain injury * Cardiovascular complications * Pulmonary complications * Metabolic dysfunction * Continued use of anti-spasticity medications * Previously diagnosed obstructive sleep apnea

Contact & Investigator

Central Contact

Milap Sandhu, PhD, PT

✉ msandhu@sralab.org

📞 312-238-6529

Principal Investigator

Milap Sandhu, PT, PhD

PRINCIPAL INVESTIGATOR

Shirley Ryan AbilityLab

Frequently Asked Questions

Who can join the NCT07739992 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 75 Years, studying Spinal Cord Injuries (SCI). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07739992 currently recruiting?

Yes, NCT07739992 is actively recruiting participants. Contact the research team at msandhu@sralab.org for enrollment information.

Where is the NCT07739992 trial being conducted?

This trial is being conducted at Chicago, United States.

Who is sponsoring the NCT07739992 clinical trial?

NCT07739992 is sponsored by Milap Sandhu. The principal investigator is Milap Sandhu, PT, PhD at Shirley Ryan AbilityLab. The trial plans to enroll 40 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology