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Effects of 4-AP on Functional SCI Recovery

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Shirley Ryan AbilityLab

Status and phase

Enrolling
Early Phase 1

Conditions

Spinal Cord Injury

Treatments

Other: Placebo drug
Drug: Dalfampridine
Behavioral: Exercise training
Other: STDP stimulation

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05447676
R35NS122336 (U.S. NIH Grant/Contract)
STU00215984

Details and patient eligibility

About

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.

Full 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.

Enrollment

44 estimated patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male and females between ages 18-85 years
  • SCI at least 4 weeks post injury
  • Spinal Cord injury at or above L2
  • ASIA A,B,C, or D, complete or incomplete
  • Possess the following abilities
  • The ability to perform a small visible contraction with dorsiflexion and hip flexor muscles

Exclusion criteria

  • Uncontrolled medical problems including pulmonary, cardiovascular or orthopedic disease
  • Any history of renal impairment
  • Any debilitating disease prior to the SCI that caused exercise intolerance
  • Premorbid, ongoing major depression or psychosis, altered cognitive status
  • History of head injury or stroke
  • Vascular, traumatic, tumoral, infectious, or metabolic lesion of the brain, even without history of seizure, and without anticonvulsant medication
  • History of seizures or epilepsy
  • Receiving drugs acting primarily on the central nervous system, which lower the seizure threshold (see appendix 2)
  • Pregnant females
  • If a women of child bearing age is unsure of the pregnancy, and does not want to take the pregnancy test Ongoing cord compression or a syrinx in the spinal cord or who suffer from a spinal cord disease such as spinal stenosis, spina bifida, MS, or herniated disk
  • Metal plate in skull
  • Individuals with scalp shrapnel, cochlear implants, or aneurysm clips
  • Individuals taking Bupropion, Dolutegravir, Lacosamide, Trilaciclib, or PR Interval prolonging drugs

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

44 participants in 3 patient groups, including a placebo group

Dalfampridine (4-AP)+STDP+training
Active Comparator group
Description:
The effects of the functional recovery of the lower-limb muscles will be determined after 10 sessions of 4-AP, STDP stimulation and training.
Treatment:
Other: STDP stimulation
Behavioral: Exercise training
Drug: Dalfampridine
Placebo+STDP+training
Placebo Comparator group
Description:
The effects of the functional recovery of the lower-limb muscles will be determined after 10 sessions of placebo drug, STDP stimulation and training.
Treatment:
Other: STDP stimulation
Behavioral: Exercise training
Other: Placebo drug
Dalfampridine (4-AP)+STDP+training for extended sessions
Experimental group
Description:
The long-term effects of the functional recovery of the lower-limb muscles will be determined after 40 sessions of 4-AP, STDP stimulation and training.
Treatment:
Other: STDP stimulation
Behavioral: Exercise training
Drug: Dalfampridine

Trial contacts and locations

1

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Central trial contact

Monica A Perez, PT, PhD; Sri Ramya Vemulakonda, M.B.B.S

Data sourced from clinicaltrials.gov

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