Spinal Cord Injury Clinical Trials
42 studies are recruiting for spinal cord injury in the United States right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
Search these by distance from you
By city
Studies now recruiting
-
CBD for Lower Urinary Tract Dysfunction in Spinal Cord Injury
The goal of this feasibility study is to learn whether Cannabidiol (CBD) can improve urinary incontinence and other symptoms in people with recent spinal cord injury (SCI). Participants will take Epidiolex (purified CBD) for 90 days
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- University of Wisconsin - Madison, Madison, Wisconsin
- Run by
- University of Wisconsin, Madison
-
mSCI: Mobile Health App for Veterans With SCI and Caregivers
Caregivers of persons with Spinal Cord Injury (SCI) face increased risk of psychological distress, health problems, reduced quality of life, relationship strain, and restrictions in social and work participation. Military caregivers (Family Caregivers of wounded or disabled Veterans) reported simil…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University of Pittsburgh, Pittsburgh, Pennsylvania
- Run by
- University of Pittsburgh
-
Safety and Feasibility of Intranasal Insulin in Patients With Spinal Cord Injury
The purpose of this study is to find out whether insulin, a drug approved by the FDA for the treatment of diabetes mellitus, is safe when administered as a nasal spray (intranasally) to people who have experienced a spinal cord injury. While insulin nasal spray has been shown to be safe in many pat…
- Stage
- Phase 1
- Ages
- 18 to 84
- Site
- HealthPartners Neuroscience Center, Saint Paul, Minnesota
- Run by
- HealthPartners Institute
-
Paired Stimulation Plasticity for Motor Recovery in Humans With and Without Spinal Cord Injury
This study will investigate how aging and spinal cord injury (SCI) affect the transmission and plasticity of the corticospinal and reticulospinal tracts, which are important pathways for motor control. The study includes two experiments. Experiment 1 will assess corticospinal and reticulospinal tra…
- Stage
- Not phased
- Ages
- 19 to 85
- Site
- Shirley Ryan Abilitylab, Chicago, Illinois
- Run by
- Shirley Ryan AbilityLab
-
Vibrant Capsule for Spinal Cord Injury Neurogenic Bowel Dysfunction
The goal of this study is to test the safety and effectiveness of Vibrant capsules in spinal cord injury patients with neurogenic bowel.
- Stage
- Not phased
- Ages
- 21 and older
- Site
- TIRR Memorial Hermann, Houston, Texas
- Run by
- The University of Texas Health Science Center, Houston
-
Male Fertility Program
Following spinal cord injury, most men are infertile and require medical assistance to father children. The conditions that contribute to their infertility are erectile dysfunction, ejaculatory dysfunction, and semen abnormalities. The Miami Project Male Fertility Program is a research study design…
- Stage
- Not phased
- Ages
- 18 to 50
- Site
- The Maimi Project to Cure Paralysis, Miami, Florida
- Run by
- University of Miami
-
Exciflex Electroceutical Banadage for Chronic Wound Therapy
Objectives: The study objective is to carry a pilot clinical assessment comparing the exciflex bandage to standard of care (SoC) for ischemic wounds and will involve participants who are Veterans with lower extremity ischemic wounds. Research Plan: The study will employ a randomized repeated measur…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Louis Stokes VA Medical Center, Cleveland, OH, Cleveland, Ohio
- Run by
- VA Office of Research and Development
-
Psilocybin to Treat Depression in Spinal Cord Injury
The main goal of this study is to determine if psilocybin is safe for use in people with SCI. The study will measure how people with SCI respond to three psilocybin doses: low (5mg), medium (10mg), and high (25mg). The main question the study aims to answer is: does psilocybin increase the number a…
- Stage
- Phase 1
- Ages
- 22 and older
- Site
- James J. Peters Department of Veterans Affairs Medical Center, The Bronx, New York
- Run by
- James J. Peters Veterans Affairs Medical Center
-
Understanding and Enhancing Human Health and Movement
By doing this study, investigators hope to learn how electrical stimulation can improve human movement, biomechanics, and function and to gather information on the safety and effectiveness of an implanted electrical stimulation system after paralysis from spinal cord injury, stroke, multiple sclero…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Louis Stokes Cleveland VA Medical Center, Cleveland, Ohio
- Run by
- Louis Stokes VA Medical Center
-
Motoneuron Recruitment and Motor Evoked Potential Up-Conditioning (MEP) in Spinal Cord Injury (SCI)
The purpose of this research study is to examine the effect of a brain stimulation training to improve the function of brain-spinal cord- muscle connections. Because brain-to-muscle pathways are very important in our movement control, restoring function of these pathways may improve movement proble…
- Stage
- Not phased
- Ages
- 18 to 80
- Site
- Medical University of South Carolina, Charleston, South Carolina
- Run by
- Medical University of South Carolina
-
At-Home Genital Nerve Stimulation for SCI Bowel
The purpose of this study is to test whether electrical stimulation of the skin in the pelvic area (near the genitals) can reduce the reflexes that cause bowel accidents in people with spinal cord injuries. Current bowel treatments either involve diet and medications or surgery. This study will eva…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- MetroHealth Center for Rehabilitation Research, Cleveland, Ohio
- Run by
- MetroHealth Medical Center
-
Treatment of Sleep Apnea in Patients With Cervical Spinal Cord Injury
This study will investigate potential therapeutic approaches for sleep-disordered breathing (SDB) in patients with chronic cervical spine injury (>6 months post-injury).
- Stage
- Phase 4
- Ages
- 18 to 89
- Site
- John D. Dingell VA Medical Center, Detroit, Michigan
- Run by
- John D. Dingell VA Medical Center
-
Pilot Study Exploring the Effects of Rhythmic Auditory Stimulation on Gait in People With Motor Incomplete Spinal Cord Injury
This pilot study aims to evaluate the feasibility and preliminary efficacy of a wearable rhythmic auditory stimulation system, MedRhythms, for improving gait parameters in patients with motor incomplete SCI. Up to 15 participants aged 18 years or older with non-progressive SCI will be enrolled. Par…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- UC Davis Point West, Sacramento, California
- Run by
- University of California, Davis
-
Pilot Study of Galantamine to Treat Metabolic Syndrome in People With Chronic Traumatic Spinal Cord Injury (SCI)
The purpose of this research study is to measure the tolerability and preliminary efficacy of a drug, galantamine, to treat metabolic syndrome (MetS) by reducing circulating inflammation in people with spinal cord injury (SCI). Galantamine is FDA-approved for the treatment of Alzheimer's disease. H…
- Stage
- Phase 2
- Ages
- 21 to 75
- Site
- Northwell Health, Manhasset, New York
- Locations
- 3 in total
- Run by
- Northwell Health
-
Tele-Exercise to Promote Empowered Movement in Individuals With Spinal Cord Injury
To achieve our specific aims and hypotheses we will conduct a parallel group mixed methods randomized control trial comparing participation in the TEEMS program with exercise via asynchronous video library equivalent (control). The use of mixed methods will allow for the integration of quantitative…
- Stage
- Not phased
- Ages
- 18 to 75
- Site
- Drexel University Health Science Building, Philadelphia, Pennsylvania
- Run by
- Drexel University
-
Cortical Recording and Stimulating Array Brain-Machine Interface
The purpose of this research study is to demonstrate the safety and efficacy of using two CRS Arrays (microelectrodes) for long-term recording of brain motor cortex activity and microstimulation of brain sensory cortex.
- Stage
- Not phased
- Ages
- 22 to 70
- Site
- University of Chicago, Chicago, Illinois
- Locations
- 2 in total
- Run by
- Michael Boninger
-
The International Spinal Cord Injury Blood Biomarker Longitudinal Evaluation (I-SCRIBBLE) Study
To determine the accuracy of serum NF-L and GFAP levels (ie the biomarkers) at different time points postinjury for predicting the severity of neurologic impairment at 6 months postinjury as either motor complete (AIS grade A/B) or motor incomplete (AIS grade C/D) a group of patients who suffer tra…
- Stage
- Not phased
- Ages
- 19 and older
- Site
- Medical College of Wisconsin, Milwaukee, Wisconsin
- Locations
- 8 in total
- Run by
- AO Foundation, AO Spine
-
Clinical Outcome Assessment for AT & BCI
Many individuals with severe motor impairments rely on Assistive Technologies (ATs) or Brain-Computer Interfaces (BCIs) to interact with digital devices such as their computers. Clinicians and researchers currently lack a common framework to objectively quantify how much a given AT or BCI improves …
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Shirley Ryan AbilityLab, Chicago, Illinois
- Run by
- Shirley Ryan AbilityLab
-
Non-invasive Spinal Cord Stimulation and Blood Pressure Regulation After Spinal Cord Injury
The goal of this clinical trial is to learn if non-invasive spinal cord stimulation intervention improves blood pressure regulation in individuals with chronic spinal cord injury. The main questions it aims to answer are: * Can site specific spinal cord stimulation enhance blood pressure regulation…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Frazier Rehabilitation Institute, Louisville, Kentucky
- Locations
- 2 in total
- Run by
- University of Louisville
-
Neuromodulation to Improve Grasping Function After SCI
The goal of this study is to restore the activities of late descending signals with a noninvasive stimulation approach in combination with hand motor training to improve hand function in persons with cervical SCI. The main question it aims to answer is if the inputs to late descending signals above…
- Stage
- Not phased
- Ages
- 18 to 75
- Site
- The State University of New York at Buffalo, Buffalo, New York
- Run by
- State University of New York at Buffalo
-
Virtual Peer Coaching in Manual Wheelchair Skills
The objective of this study is to determine the effectiveness of remote manual wheelchair skills training program. First, peer coaches will be enrolled and trained. Then, trainees will be enrolled into one of three interventions: intervention with remote feedback (Group 1), and a wait list control …
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University of Pittsburgh, Pittsburgh, Pennsylvania
- Run by
- University of Pittsburgh
-
MEP Up-conditioning to Target Corticospinal Plasticity
Individuals with chronic cervical spinal cord injury will complete a 10-week training protocol where participants receive non-invasive brain stimulation and feedback on the size of the corresponding muscle response (wrist extensor). Investigators will assess the impact of the brain stimulation trai…
- Stage
- EARLY_Phase 1
- Ages
- 18 and older
- Site
- Medical University of South Carolina, Charleston, South Carolina
- Run by
- Medical University of South Carolina
-
Shockwave for Elbow and Wrist Spasticity in People With Spinal Cord Injury
Approximately 305,000 people live with a spinal cord injury (SCI) in the United States. Sixty percent of these individuals have tetraplegia, which can cause significant dysfunction of the arms and hands. One of the consequences of SCI is spasticity - involuntary activation of muscles that can hinde…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Kessler Foundation, West Orange, New Jersey
- Run by
- Kessler Foundation
-
CE-STAND: Cervical Epidural STimulation After Neurologic Damage
CE-STAND aims to address three areas under-represented in research: chronic, cervical, and autonomic dysfunction. It is both significant and highly impactful, as treating autonomic dysfunction could substantially improve function and quality of life (QoL) in chronic cervical SCI patients.
- Stage
- Phase 1
- Ages
- 22 and older
- Site
- University of Minnesota, Minneapolis, Minnesota
- Run by
- University of Minnesota
-
Chronic Transcutaneous Stimulation to Promote Motor Function and Recovery in Individuals With Paralysis or Paresis
This is an early feasibility trial to determine whether transcutaneous neuromuscular electrical stimulation, with or without transcutaneous spinal cord stimulation, using an investigational neurostimulation device improves functional arm/hand movements in individuals with paralysis or paresis due t…
- Stage
- EARLY_Phase 1
- Ages
- 18 to 75
- Site
- Northwell Health's The Feinstein Institute for Medical Research, Manhasset, New York
- Run by
- Northwell Health
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.
Paid placement. Some studies pay us when someone asks to be connected to them. Those are labelled Sponsored wherever they appear, and they only appear when they match what you were actually looking for.