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Two Devices for Reflex Voiding Following Spinal Cord Injury

Primary Purpose

Spinal Cord Injury, Urinary Incontinence

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Vibrator
Anal dilator
Sponsored by
US Department of Veterans Affairs
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Spinal Cord Injury focused on measuring electric stimulation, urethral obstruction, urodynamics, urology

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

Male Veterans using Hines VA Hospital SCI Service that have upper motor neuron injuries

Exclusion Criteria:

  • Can voluntarily control their urination
  • Surgically removed external urethral sphincter in men or replaced bladder
  • Any implanted devices in the lower urinary tract
  • Female
  • Urinary tract infection in the prior 3 months or untreated urinary tract infection, or bladder pathology such as a tumor or stones
  • History of autonomic dysreflexia
  • Anal inflammation or pathology
  • Use of Indwelling (Foley) catheter as the primary method of bladder management; note patients will be included if they only occasionally use a Foley catheters; for example, during traveling
  • Not under 18 or over 70 years old and in good health
  • Less than 3-months after injury and before the return of bladder reflexes
  • Lower motor neuron spinal cord injury
  • Not competent to understand the study and the consent and willing to participate in study.

Sites / Locations

  • Edward Hines, Jr. VA Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Arm 1

Arm Description

Use a vibrator on the patient's bottom to determine if it will induce a bladder contraction; Use an anal dilator to determine if urethral relaxation will occur

Outcomes

Primary Outcome Measures

Number of Participants With a Change in Bladder Pressure
Measured via pressure catheter in bladder with a pressure transducer
Number of Participants With a Change in External Urethral Pressure
Measured via balloon catheter
Number of Participants With a Change in Anal Sphincter Pressure
Measured via balloon catheter
Number of Participants With a Urethral Sphincter Contractions

Secondary Outcome Measures

Full Information

First Posted
April 1, 2008
Last Updated
November 4, 2014
Sponsor
US Department of Veterans Affairs
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1. Study Identification

Unique Protocol Identification Number
NCT00662207
Brief Title
Two Devices for Reflex Voiding Following Spinal Cord Injury
Official Title
Two Devices for Reflex Voiding Following SCI: Urodynamic Evaluation
Study Type
Interventional

2. Study Status

Record Verification Date
November 2014
Overall Recruitment Status
Completed
Study Start Date
October 2008 (undefined)
Primary Completion Date
October 2009 (Actual)
Study Completion Date
October 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
US Department of Veterans Affairs

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this investigation is to evaluate methods in spinal cord injured individuals to improve reflex urination. Anal dilation will be investigated to reduce high urethral resistance and a vibrator on the patient's bottom will be tested to induce more sustained bladder contractions for better bladder emptying.
Detailed Description
Catheters are often used by individuals emptying their bladder following spinal cord injury. Reflex voiding is one of the bladder emptying methods, and it relies on spontaneous bladder contractions for voiding. These contractions occur with normal bladder filling or can be induced with suprapubic tapping and hair pulling. Poor voiding responses with reflex voiding can occur because of unwanted contractions of the urethra during bladder contractions and/or unsustained bladder contractions that result in high residual urine. The focus of this investigation is methods to reduce the high urethral resistance and to induce more sustained bladder contractions. Obj.1. Measure pelvic floor contractile activity including the pelvic floor relaxation response (urethral and anal pressures, and EMG and the bulbocavernosus reflex) during dilation of the anus with digits or a balloon for 60 sec at diameters of 2, 3.5 and 5 cm. Obj. 2. Measure urodynamic parameters (urethral and anal pressures, EMG, urine flow rates and bladder pressure) and compare three somatic methods of inducing bladder contractions, which are vibration (3 mm conducted at 100 strokes per second) at suprapubic and perineum (between the scrotum and anus) locations and tapping/suprapubic hair pulling. Conduct procedures using 80% of cystometric capacity and define a responder to any of the three interventions as an increase of 10 cm H20 pressure or greater. For nonresponders go to objective 4. Obj. 3. For responders to Ob. 2, further evaluate effects of perineum vibration by conducting comparisons with (1) anal dilation to no dilation; (2) A vibration stroke length of 1.5 mm to 3 mm; (3) A bladder volume of 50% cystometric capacity to 80%. Obj. 4. Compare the urodynamic responses to spontaneous bladder contractions induced by bladder filling (cystometry) with and without anal dilation. Obj. 5. Conduct a human factors assessment. Determine problems with use of the current perineum vibration and anal dilation devices. Evaluate if curving the tip of the insertion device for the anal dilator would facilitate insertion and if the use of a plastic bag would improve hygiene. Discuss features important for a user-friendly home-use device. Design & Methods: All objectives will be conducted during a single, urodynamic, testing protocol. Fifteen male SCI patients with upper-motor-neuron injuries will be enrolled. Urodynamic responses are our primary measure. These include urethral and anal sphincter pressures and anal surface EMG, bladder contractions including peak pressure and duration of pressure, voiding responses including peak voiding rate and duration of voiding. These measures will be evaluated during anal dilation and perineum vibration methods alone and in combination. Anal dilation protocols will include random and duplicated testing. Vibration methods will only be done once to limit the risk of autonomic dysreflexia. Analysis of variance followed by Student-Neuman-Keuls post hoc test will be conducted to assess significant differences. Importance of Findings: Results from these studies will provide evidence for anal dilation to reduce DSD and perineum vibration to improve bladder contractions. Thus, these studies could provide important evidence for improved methods of RV for individuals with SCI. During this pilot study, subjects will not be counseled to conduct RV for their daily or regular bladder management program.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spinal Cord Injury, Urinary Incontinence
Keywords
electric stimulation, urethral obstruction, urodynamics, urology

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
3 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm 1
Arm Type
Experimental
Arm Description
Use a vibrator on the patient's bottom to determine if it will induce a bladder contraction; Use an anal dilator to determine if urethral relaxation will occur
Intervention Type
Device
Intervention Name(s)
Vibrator
Other Intervention Name(s)
perinuem vibrator
Intervention Description
A vibrator will be applied to the patient's bottom to determine if it will induce a bladder contraction
Intervention Type
Procedure
Intervention Name(s)
Anal dilator
Other Intervention Name(s)
Modified rectal balloon for anal dilation
Intervention Description
A balloon will be used for anal dilation to determine if it will result in relaxation of the pelvic floor and urethral sphincter. An anal dilator is being conduced with the balloon
Primary Outcome Measure Information:
Title
Number of Participants With a Change in Bladder Pressure
Description
Measured via pressure catheter in bladder with a pressure transducer
Time Frame
3 hour recording session
Title
Number of Participants With a Change in External Urethral Pressure
Description
Measured via balloon catheter
Time Frame
3 hour recording session
Title
Number of Participants With a Change in Anal Sphincter Pressure
Description
Measured via balloon catheter
Time Frame
3 hour recording session
Title
Number of Participants With a Urethral Sphincter Contractions
Time Frame
3 hour recording session

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male Veterans using Hines VA Hospital SCI Service that have upper motor neuron injuries Exclusion Criteria: Can voluntarily control their urination Surgically removed external urethral sphincter in men or replaced bladder Any implanted devices in the lower urinary tract Female Urinary tract infection in the prior 3 months or untreated urinary tract infection, or bladder pathology such as a tumor or stones History of autonomic dysreflexia Anal inflammation or pathology Use of Indwelling (Foley) catheter as the primary method of bladder management; note patients will be included if they only occasionally use a Foley catheters; for example, during traveling Not under 18 or over 70 years old and in good health Less than 3-months after injury and before the return of bladder reflexes Lower motor neuron spinal cord injury Not competent to understand the study and the consent and willing to participate in study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
James Walter, PhD
Organizational Affiliation
Edward Hines Jr. VA Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Edward Hines, Jr. VA Hospital
City
Hines
State/Province
Illinois
ZIP/Postal Code
60141-5000
Country
United States

12. IPD Sharing Statement

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Two Devices for Reflex Voiding Following Spinal Cord Injury

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