Recovery of Bladder and Sexual Function After Human Spinal Cord Injury

Description

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

Urinary Bladder, Neurogenic, Blood Pressure, Autonomic Dysreflexia, Bowel Incontinence

Study Overview

Study Details

Study overview

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.

Effects of Activity-Dependent Plasticity on Recovery of Bladder and Sexual Function After Human Spinal Cord Injury

Recovery of Bladder and Sexual Function After Human Spinal Cord Injury

Condition
Urinary Bladder, Neurogenic
Intervention / Treatment

-

Contacts and Locations

Louisville

University of Louisville, Louisville, Kentucky, United States, 40202

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * At least 18 years of age;
  • * AIS A to D;
  • * Neurogenic bladder and bowel dysfunction;
  • * Stable medical condition
  • * Prior Botox injections of the bladder and/or bladder augmentation surgery;
  • * Colostomy bag,
  • * Ventilator dependent;
  • * Any implanted pump (i.e. Baclofen pump, pain pump, etc.);
  • * Pregnant at the time of enrollment or planning to become pregnant during the time course of the study

Ages Eligible for Study

18 Years to 70 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Louisville,

Charles Hubscher, PhD, PRINCIPAL_INVESTIGATOR, University of Louisville

Study Record Dates

2027-01-03