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UnknownNCT05447676

Effects of 4-AP on Functional SCI Recovery

Effects of 4-AP on Functional Recovery After Spinal Cord Injury

Status
Unknown
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
44 (estimated)
Sponsor
Shirley Ryan AbilityLab · Academic / Other
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to test a strategy to potentiate functional recovery of lower limb motor function in individuals with spinal cord injury (SCI). The FDA approved drug, Dalfampridine (4-AP). 4-AP will be used in combination of Spike-timing-dependent plasticity (STDP) stimulation and STDP stimulation with limb training.

Detailed description

Currently, research has shown that 4-AP has a positive effect on sensory and motor function rehabilitation in humans with chronic SCI in addition to decreasing recorded spasticity, increased sensation, and decreased pain. Utilizing limb training to promote recovery of motor function is enhanced by eliciting STDP in the limbs. An important strength of this aim is the combination of training and STDP, which aims at enhancing the beneficial effects of motor training by promoting plasticity in the corticospinal pathway. We hypothesize that introducing 4-AP into the STDP stimulation and STDP stimulation with lower-limb training will further improve motor function rehabilitation in patients with chronic SCI.

Conditions

Interventions

TypeNameDescription
DRUGDalfampridineThe study drug (4-AP) will be administered as a 10 mg dose.
OTHERPlacebo drugThe pharmacy will also provide a placebo drug that looks identical to 4-AP to verify participants and therapists do not know who is receiving the drug and who is receiving the placebo.
OTHERSTDP stimulationPaired stimulation will be given to the spinal cord and to peripheral nerves so that the signals are received at the spinal cord at a specific interval.
BEHAVIORALExercise trainingLower-limb exercises will involve over-ground walking, treadmill, walking and stair climbing training.

Timeline

Start date
2022-06-30
Primary completion
2024-06-30
Completion
2025-06-30
First posted
2022-07-07
Last updated
2023-06-22

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05447676. Inclusion in this directory is not an endorsement.