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Improving the Efficacy of Sacral Nerve Stimulation for Fecal Incontinence by Alteration of Stimulation Parameters

Primary Purpose

Fecal Incontinence

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Medtronic InterStim / InterStim II
Sponsored by
University of Aarhus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fecal Incontinence focused on measuring Idiopathic Fecal Incontinence, Fecal Incontinence, Sacral Nerve Stimulation, Sacral Nerve Neuromodulation

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Informed Consent
  • Diagnosed with idiopathic faecal incontinence,incontinence with minor (≤60 degrees) sphincteric defects or incontinence following sphincter repair.
  • Medtronic Interstim IPG(pacemaker)implanted for more than 6 months
  • minimum one incontinence episodes pr. week during ongoing SNS-therapy

Exclusion Criteria:

  • Colorectal surgery after IPG-implantation
  • Pregnancy or breastfeeding
  • Anal/perianal pain or discomfort
  • Patients who are not deemed able to follow the planned testing program, including mental illness or mentally unstable patients
  • Medication with known effects on gastrointestinal motility, thyroid disease, diabetes, coeliac, neurological disorders.
  • Spinal cord injury
  • Irritable Bowel Syndrome

Sites / Locations

  • Anal Physiology Laboratory, Surgical Research Section 900, Aarhus University Hospital
  • St. Marks Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm Type

Active Comparator

Experimental

Experimental

Experimental

Experimental

Arm Label

Standard settings

Experimental Setting 1

Experimental setting 2

Experimental setting 3

Experimental setting 4

Arm Description

Amplitude: Sensory threshold Frequency:14 Hz Pulse width 210 μsec

Amplitude: Sensory threshold Frequency:6.9 Hz Pulse width 210 μsec

Amplitude: Sensory threshold Frequency:31 Hz Pulse width 210 μsec

Amplitude: Sensory threshold Frequency:14 Hz Pulse width 330 μsec

Amplitude: Sensory threshold Frequency:14 Hz Pulse width 90 μsec

Outcomes

Primary Outcome Measures

Quality of life changes
Quality of life will be recorded by means of Rockwood faecal incontinence quality of life score. A total of five evaluations will be made every fourth week in the twenty week protocol perioed.

Secondary Outcome Measures

Number of incontinence episodes
Assess number of incontinence episodes, by means of bowel habit diary. Four week bowel habit diary will be evaluated five times during the twenty-week protocol perioed.
Days with faecal soiling
By means of a four week bowel habit diary
Days with faecal urgency.
By means of a four week bowel habit diary
Wexner incontinence score
St. Marks Incontinence score
Assess changes in anorectal volume and pressure with different pacemaker settings
Resting, maximal anal sphincter pressure and rectal filling(first sensation, urge to defacate and maximal tolerabel volume(Air))pressure will be measured with different pacemaker settings. In total five evaluations will be made in the twenty week protocol perioed.

Full Information

First Posted
December 3, 2010
Last Updated
November 9, 2011
Sponsor
University of Aarhus
Collaborators
London North West Healthcare NHS Trust
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1. Study Identification

Unique Protocol Identification Number
NCT01254695
Brief Title
Improving the Efficacy of Sacral Nerve Stimulation for Fecal Incontinence by Alteration of Stimulation Parameters
Official Title
Improving the Efficacy of Sacral Nerve Stimulation for Fecal Incontinence by Alteration of Stimulation Parameters
Study Type
Interventional

2. Study Status

Record Verification Date
November 2011
Overall Recruitment Status
Completed
Study Start Date
July 2010 (undefined)
Primary Completion Date
March 2011 (Actual)
Study Completion Date
June 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Aarhus
Collaborators
London North West Healthcare NHS Trust

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Faecal incontinence is a devastating condition affecting 2,2 to 5 % of the adult population. The magnitude of the problem is probably underestimated. Sacral nerve stimulation (SNS), has over the last decade given hope to patient failing conservative treatment. Some patient do not have optimal continence after SNS-therapy. This study aims to identify optimal stimulation parameters - that will improve the functional outcome of SNS-therapy thru a double blinded randomized cross-over study.
Detailed Description
Faecal incontinence is a devastating condition affecting daily living and has major influences on quality of life. Faecal incontinence affects 2,2 to 5 % of the adult population. The magnitude of the problem is probably underestimated, because most patients don't discuss this affliction with their general practitioner. A new treatment, SNS has over the last decade given new hope to these patients. But a group of these patients has minor effect of the treatment - despite a satisfactory test-stimulation period. This study aims to identify optimal stimulation parameters that will improve patient continence and quality of life. Four different stimulation parameters will be tested through a double blind, randomized crossover study - standard stimulation parameters (frequency: 14 Hz, pulse width 210 microsec.) will serve as control stimulation. The study includes five arms that will be tested in a randomized order. Each arm will be tested for four weeks in which the patient fill in bowel habit diaries and standardized questionnaires. The first week in each period will not be evaluated - is serves as a wash-out period. Before any pacemaker changes anorectal manometry and rectal filling tests will be performed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fecal Incontinence
Keywords
Idiopathic Fecal Incontinence, Fecal Incontinence, Sacral Nerve Stimulation, Sacral Nerve Neuromodulation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
15 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard settings
Arm Type
Active Comparator
Arm Description
Amplitude: Sensory threshold Frequency:14 Hz Pulse width 210 μsec
Arm Title
Experimental Setting 1
Arm Type
Experimental
Arm Description
Amplitude: Sensory threshold Frequency:6.9 Hz Pulse width 210 μsec
Arm Title
Experimental setting 2
Arm Type
Experimental
Arm Description
Amplitude: Sensory threshold Frequency:31 Hz Pulse width 210 μsec
Arm Title
Experimental setting 3
Arm Type
Experimental
Arm Description
Amplitude: Sensory threshold Frequency:14 Hz Pulse width 330 μsec
Arm Title
Experimental setting 4
Arm Type
Experimental
Arm Description
Amplitude: Sensory threshold Frequency:14 Hz Pulse width 90 μsec
Intervention Type
Device
Intervention Name(s)
Medtronic InterStim / InterStim II
Other Intervention Name(s)
Medtronic InterStim, Medtronic InterStim II
Intervention Description
Standard stimulation (Amplitude: sensory threshold, frequency 14 Hz, Pulsewidth 210 microsec.) will be compared wiht experimental setting 1,2,3,4
Primary Outcome Measure Information:
Title
Quality of life changes
Description
Quality of life will be recorded by means of Rockwood faecal incontinence quality of life score. A total of five evaluations will be made every fourth week in the twenty week protocol perioed.
Time Frame
Will be assessed every four weeks during a twenty-week period
Secondary Outcome Measure Information:
Title
Number of incontinence episodes
Description
Assess number of incontinence episodes, by means of bowel habit diary. Four week bowel habit diary will be evaluated five times during the twenty-week protocol perioed.
Time Frame
Will be assessed every four weeks durring a twenty-week period
Title
Days with faecal soiling
Description
By means of a four week bowel habit diary
Time Frame
Will be assessed every four weeks during a twenty-week period
Title
Days with faecal urgency.
Description
By means of a four week bowel habit diary
Time Frame
Will be assessed every four weeks during a twelve-week period
Title
Wexner incontinence score
Time Frame
Will be assessed every four weeks during a twenty-week period
Title
St. Marks Incontinence score
Time Frame
Will be assessed every four weeks during a twenty-week period
Title
Assess changes in anorectal volume and pressure with different pacemaker settings
Description
Resting, maximal anal sphincter pressure and rectal filling(first sensation, urge to defacate and maximal tolerabel volume(Air))pressure will be measured with different pacemaker settings. In total five evaluations will be made in the twenty week protocol perioed.
Time Frame
Will be assessed every four weeks during a twenty-week period

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Informed Consent Diagnosed with idiopathic faecal incontinence,incontinence with minor (≤60 degrees) sphincteric defects or incontinence following sphincter repair. Medtronic Interstim IPG(pacemaker)implanted for more than 6 months minimum one incontinence episodes pr. week during ongoing SNS-therapy Exclusion Criteria: Colorectal surgery after IPG-implantation Pregnancy or breastfeeding Anal/perianal pain or discomfort Patients who are not deemed able to follow the planned testing program, including mental illness or mentally unstable patients Medication with known effects on gastrointestinal motility, thyroid disease, diabetes, coeliac, neurological disorders. Spinal cord injury Irritable Bowel Syndrome
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jakob k Jakobsen, MD.
Organizational Affiliation
Anal Physiology Laboratory, Surgical Research Section 900, Aarhus University Hospital, Denmark
Official's Role
Principal Investigator
Facility Information:
Facility Name
Anal Physiology Laboratory, Surgical Research Section 900, Aarhus University Hospital
City
Aarhus
State/Province
Aarhus C
ZIP/Postal Code
8200
Country
Denmark
Facility Name
St. Marks Hospital
City
London
State/Province
Harrow - Middlesex
ZIP/Postal Code
HA1 3UJ
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
22961528
Citation
Duelund-Jakobsen J, Dudding T, Bradshaw E, Buntzen S, Lundby L, Laurberg S, Vaizey C. Randomized double-blind crossover study of alternative stimulator settings in sacral nerve stimulation for faecal incontinence. Br J Surg. 2012 Oct;99(10):1445-52. doi: 10.1002/bjs.8867.
Results Reference
derived

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Improving the Efficacy of Sacral Nerve Stimulation for Fecal Incontinence by Alteration of Stimulation Parameters

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