NCT05447676

Effects of 4-AP on Functional SCI Recovery

Effects of 4-AP on Functional Recovery After Spinal Cord Injury
Shirley Ryan AbilityLab·Phase 1·ClinicalTrials.gov·drugRecruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Spinal Cord Injury
Drug/Device/Intervention
Dalfampridine
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
Shirley Ryan AbilityLab
Location
Chicago, United States of America
Timeline & enrollment
Phase
Phase 1
Start date
Jun 30, 2022
End date
Jun 01, 2025
Enrollment
44 participants
Primary outcome

Change in TMEPs,Change in MVC

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.

ICD-10 classifications
Sequelae of injury of spinal cordOther injury of lumbar spinal cordInjury of spinal cord, level unspecifiedOther and unspecified injuries of thoracic spinal cordOther and unspecified injuries of cervical spinal cord
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT05447676
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT05447676 through Pure Global AI's free database. This Phase 1 trial is sponsored by Shirley Ryan AbilityLab and is currently Recruiting. The study focuses on Spinal Cord Injury. Target enrollment is 44 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.