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"UroMonitor Trial" in Spinal Cord Injury.

NCT04800523 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2021-10-28

No results posted yet for this study

Summary

This study aims to determine if a non-functioning UroMonitor device can be safely inserted, monitored, and removed in patients with SCI.

Conditions

  • Spinal Cord Injuries

Interventions

DEVICE

UroMonitor System

Implantable device to wirelessly and without catheters monitor the neurogenic bladder on an ambulatory basis

Sponsors & Collaborators

  • United States Department of Defense

    collaborator FED

  • University of British Columbia

    lead OTHER

Principal Investigators

  • Brian Kwon, MD · University of British Columbia

Study Design

Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
17 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-10-31
Primary Completion
2022-12-31
Completion
2023-03-15

Countries

  • Canada

Study Locations

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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 NCT04800523 on ClinicalTrials.gov