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SCI Patient for Spinal Cord Injury (ISI Trial)

N/A
Recruiting
Led By David Borton, PhD
Research Sponsored by Rhode Island Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 8 months
Awards & highlights

ISI Trial Summary

This trial is testing a new device to help spinal cord injury patients regain function in their lower limbs. The device is implanted and then various tests are done to assess the patients' progress.

Eligible Conditions
  • Spinal Cord Injury

ISI Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~8 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 8 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Evaluate safety issues
Secondary outcome measures
Functional Outcome Measures
Neurological Outcome Measures

ISI Trial Design

1Treatment groups
Experimental Treatment
Group I: SCI PatientExperimental Treatment1 Intervention
Complete or Incomplete Spinal Cord Injury (SCI) patients with Asia Impairment Score (AIS) of A or B between the levels of C7/T1 and T10

Find a Location

Who is running the clinical trial?

Rhode Island HospitalLead Sponsor
261 Previous Clinical Trials
69,003 Total Patients Enrolled
US Department of Veterans AffairsFED
870 Previous Clinical Trials
495,944 Total Patients Enrolled
Brown UniversityOTHER
456 Previous Clinical Trials
558,253 Total Patients Enrolled
~1 spots leftby Jun 2025
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