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Noninvasive Neuroprosthesis for Autonomic Recovery After SCI

NCT04977284 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 5

Last updated 2021-07-26

No results posted yet for this study

Summary

This research study is being conducted to help explore the effects of non-invasive (non-surgical) spinal cord stimulation via sticky electrodes over the skin (transcutaneous spinal cord stimulation; TCSCS) on bowel, bladder and sexual function following spinal cord injury. Our primary aim is to determine the specific location and timing of TCSCS at various spinal cord levels in order to target bladder and bowel control (Study 1 and 2), and to assess the safety and effectiveness of TCSCS during bladder and bowel function assessments (Study 2 only). Participants may choose to participate in either Study 1 or 2.

Conditions

  • Spinal Cord Injuries

Interventions

DEVICE

DS7R, Digitimer, UK

Non-surgical spinal cord stimulation will be applied and electrical activity of muscles will be recorded.

Sponsors & Collaborators

  • Praxis Spinal Cord Institute

    collaborator OTHER

  • St. Paul's Hospital

    collaborator UNKNOWN

  • University of British Columbia

    lead OTHER

Principal Investigators

  • Andrei Krassioukov, MD, PhD · University of British Columbia

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-09-01
Primary Completion
2022-04-30
Completion
2022-04-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04977284 on ClinicalTrials.gov