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NCT06213012

Harnessing Neuroplasticity of Postural Sensorimotor Networks Using Non-Invasive Spinal Neuromodulation to Maximize Functional Recovery After Spinal Cord Injury

Recruiting now NA Last updated 30 March 2026
What this trial tests

NA trial testing Transcutaneous Spinal cord Stimulation in Spinal Cord Injuries in 60 participants. Currently enrolling.

Timeline
6 December 2023
Primary endpoint
31 August 2027
31 August 2027

Quick facts

Lead sponsorThe Methodist Hospital Research Institute
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment60
Start date6 December 2023
Primary completion31 August 2027
Estimated completion31 August 2027
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

The Methodist Hospital Research Institute

Who can join

Adults 22 to 75, any sex, with Spinal Cord Injuries or Neuromodulation. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

It has been demonstrated that the human lumbosacral spinal cord can be neuromodulated with epidural (ESS) and transcutaneous (TSS) spinal cord stimulation to enable recovery of standing and volitional control of the lower limbs after complete motor paralysis due to spinal cord injury (SCI). The work proposed herein will examine and identify distinct electrophysiological mechanisms underlying transcutaneous spinal stimulation (TSS) and epidural spinal stimulation (ESS) to define how these approaches determine the ability to maintain self-assisted standing after SCI.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Spinal Cord Injuries

Currently open trials in the same condition.

Other The Methodist Hospital Research Institute trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06213012.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing