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NCT04193709 · ClinicalTrials.gov registry record · NA
Recovery of Bladder and Sexual Function After Human Spinal Cord Injury
A NA study of Blood Pressure and Urinary Bladder, Neurogenic, sponsored by University of Louisville.
- Recruiting
- Registry status
- NA
- Development phase
- 70
- Enrollment target
- 1
- Study location
NCT04193709 is a NA study of Blood Pressure and Urinary Bladder, Neurogenic that is actively recruiting participants, run by University of Louisville. The registered enrollment target is 70 participants, below the 286-participant average among 101 other Blood Pressure trials with a reported enrollment target (76% lower). The trial reports 1 study location across 1 state.
The verdict
NCT04193709, a NA study of Blood Pressure and Urinary Bladder, Neurogenic, is actively recruiting participants, sponsored by University of Louisville.
- RECRUITING
- Registry status
- NA
- Development phase
- 70 participants
- Enrollment target
- 1
- Study location
Study Summary
This study will incorporate critical cross viscero-visceral intersystem interactions to 1) investigate in a controlled laboratory setting and then with mobile at-home monitoring the extent, severity, and frequency of occurrence of autonomic dysreflexia with respect to daily bladder and bowel function, in conjunction with identifying potential underlying mechanisms by examining urinary biomarkers for several specific vasoactive hormones, and 2) to regulate cardiovascular function therapeutically as part of bladder and bowel management using spinal cord epidural stimulation.
Conditions Studied
Interventions
- DEVICE Spinal Cord Epidural Stimulation
Study Locations (1)
Kentucky
- University of Louisville - Louisville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 70 participants |
| Start Date | 2021-01-04 |
| Est. Completion | 2027-01-03 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04193709
The ClinicalTrials.gov registry entry for NCT04193709 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 70 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 286-participant average among 101 other Blood Pressure trials with a reported enrollment target (76% lower). The listed sponsor is University of Louisville, which has 217 total studies on file at ClinicalTrials.gov.
The record links to 4 conditions, with Blood Pressure appearing as the primary indexed condition, and to 1 intervention - of which Spinal Cord Epidural Stimulation is the first listed.
NCT04193709 reports 1 study location spanning 1 distinct geographic area - top geographies include Kentucky.
Frequently Asked Questions
What is clinical trial NCT04193709 about?
NCT04193709 is a clinical study titled "Recovery of Bladder and Sexual Function After Human Spinal Cord Injury". This study will incorporate critical cross viscero-visceral intersystem interactions to 1) investigate in a controlled laboratory setting and then with mobile at-home monitoring the extent, severity, and frequency of occurrence of autonomic dysreflexia with respect to daily bladder and bowel functio...
What is the current status of trial NCT04193709?
This trial is currently recruiting. It is a NA study. The enrollment target is 70 participants. The study started on 2021-01-04. Estimated completion is 2027-01-03.
What conditions does trial NCT04193709 study?
This clinical trial studies the following conditions: Blood Pressure, Urinary Bladder, Neurogenic, Autonomic Dysreflexia, Bowel Incontinence.
What interventions are being tested in trial NCT04193709?
The interventions under investigation include: Spinal Cord Epidural Stimulation (DEVICE).
Who is sponsoring clinical trial NCT04193709?
This trial is sponsored by University of Louisville, which has 217 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04193709 being conducted?
This trial has 1 study location across Kentucky. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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