Cerebral Responses During Bilateral/Unilateral Sacral Nerve Stimulation for Idiopathic Faecal Incontinence
Primary Purpose
Regional Cerebral Blood Flow, Fecal Incontinence
Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Medtronic InterStim II - 3058
Sponsored by
About this trial
This is an interventional basic science trial for Regional Cerebral Blood Flow focused on measuring Positron emission tomography (PET), Idiopathic Faecal Incontinence, Bilateral Sacral Nerve Stimulation, Sacral Nerve Stimulation, Sacral Nervemodulation
Eligibility Criteria
Inclusion Criteria:
- 18 years or older
- Informed consent
- Idiopathic fecal incontinence or Fecal incontinence due to small sphincter defect(≤60 o)
- Permanent neuromodulator (medtronic InterStim II) bilateral implanted
- Reduction in fecal incontinence episodes of at least 50% between baseline and latest follow up with unilateral stimulation(Bowel diary card)
- Willing and competent to fill out diary cards
- MR-cerebrum before implantatation of neuromodulator
- Right-handed dominant
Exclusion Criteria:
- Colorectal/proctological surgery since IPG-implant
- Pregnancy
- Neurological diseases including spinal cord injury.
- Use of medication with known alternation of gastrointestinal motilitet (thyroid, diabetes, neuroleptica)
- Claustrofobia
- Latex allergy
Sites / Locations
- Anal Physiology Laboratory, Surgical Research Section 900, Aarhus University Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Experimental
Arm Label
Off/Off
On/On
On/Off
Arm Description
Pacemaker status: Bilateral Off for four weeks before first PET scann.
Pacemaker status: Bilateral On. PET scan one hour after activation and after four weeks continuous stimulation.
Pacemaker status: Unilateral On. PET scan one hour after activation and after four weeks continuous stimulation.
Outcomes
Primary Outcome Measures
Changes in Regional Cerebral Blood Flow with different pacemaker settings
RCBF evaluated with positron emission tomography.
Secondary Outcome Measures
Changes in continence and quality of life with different pacemaker activation.
Changes in incontinence episodes and quality of life will be correlated to changes in RCBF with different pacemaker activation.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01095029
Brief Title
Cerebral Responses During Bilateral/Unilateral Sacral Nerve Stimulation for Idiopathic Faecal Incontinence
Official Title
Cerebral Responses During Bilateral/Unilateral Sacral Nerve Stimulation for Idiopathic Faecal Incontinence - Assessed With Positron Emission Tomography Scan (PET-scan)
Study Type
Interventional
2. Study Status
Record Verification Date
March 2012
Overall Recruitment Status
Completed
Study Start Date
February 2010 (undefined)
Primary Completion Date
August 2012 (Actual)
Study Completion Date
July 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Aarhus
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to determine whether Sacral Nerve Stimulation (SNS) for idiopathic faecal incontinence affect cortical and deep brain activity in an acute and chronically stimulation model. Furthermore the association between brain activity and unilateral/bilateral SNS will be studied in each patient. Brain activity will be studied by use of positron emission tomography.
Detailed Description
Faecal incontinence is a devastating condition affecting daily living and quality of life. A new treatment Sacral Nerve Stimulation (SNS) has over the last decade given new hope to these patients. In Europe SNS is routinely offered to patients not archiving satisfactory continence result with standard non-surgical treatments. SNS is electrical stimulation of the sacral nerve root(s2,3 or 4). Stimulation of this nerve roots results in improved continence. The mechanism of action is at present not well described. Recent studies have shown that the effect of SNS is by means a neuromodulation in the central nervous system, whereas direct stimulation of efferent nerves to the anal sphincter and the pelvic floor has less significance.
The aim of this study is to describe changes in regional cerebral blood flow (RCBF), with positron emission tomography (PET), in patients implanted bilaterally with sacral neuromodulators with the indication idiopathic faecal incontinence.
RCBF in three deferent stimulations settings will be compared. PET will be performed before and one hour after changes in the activity status of the pacemakers. Four weeks prior to the first scan, patients are informed to switch both neurostimulator off. PET will be performed with the pacemaker settings: OFF/OFF (Stimulation status of left/right pacemaker), On/Off and On/On. The order of the On/OFF and On/On period will be random. Unilateral stimulation will be performed with the pacemaker there has the best efficacy, determined prior to study enrolment. The interval between these three pacemaker settings is four weeks. Four weeks prior to each PET scan the patients fill in bowel habit diaries, bowel habit questionnaires and quality of life assessments.
The association between continence and changes in RCBF will be studied. Additional RCBF and quality of life will be compared.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Regional Cerebral Blood Flow, Fecal Incontinence
Keywords
Positron emission tomography (PET), Idiopathic Faecal Incontinence, Bilateral Sacral Nerve Stimulation, Sacral Nerve Stimulation, Sacral Nervemodulation
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
10 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Off/Off
Arm Type
Experimental
Arm Description
Pacemaker status: Bilateral Off for four weeks before first PET scann.
Arm Title
On/On
Arm Type
Experimental
Arm Description
Pacemaker status: Bilateral On. PET scan one hour after activation and after four weeks continuous stimulation.
Arm Title
On/Off
Arm Type
Experimental
Arm Description
Pacemaker status: Unilateral On. PET scan one hour after activation and after four weeks continuous stimulation.
Intervention Type
Device
Intervention Name(s)
Medtronic InterStim II - 3058
Intervention Description
Stimulation with optimal pacemaker settings unilateral and bilateral with standard pacemaker settings: Amplitude sensory treshold, frequency 14 Hz and impulsduration 210 μsec.
Primary Outcome Measure Information:
Title
Changes in Regional Cerebral Blood Flow with different pacemaker settings
Description
RCBF evaluated with positron emission tomography.
Time Frame
12 weeks after study enrolment
Secondary Outcome Measure Information:
Title
Changes in continence and quality of life with different pacemaker activation.
Description
Changes in incontinence episodes and quality of life will be correlated to changes in RCBF with different pacemaker activation.
Time Frame
12 weeks after study enrolment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
18 years or older
Informed consent
Idiopathic fecal incontinence or Fecal incontinence due to small sphincter defect(≤60 o)
Permanent neuromodulator (medtronic InterStim II) bilateral implanted
Reduction in fecal incontinence episodes of at least 50% between baseline and latest follow up with unilateral stimulation(Bowel diary card)
Willing and competent to fill out diary cards
MR-cerebrum before implantatation of neuromodulator
Right-handed dominant
Exclusion Criteria:
Colorectal/proctological surgery since IPG-implant
Pregnancy
Neurological diseases including spinal cord injury.
Use of medication with known alternation of gastrointestinal motilitet (thyroid, diabetes, neuroleptica)
Claustrofobia
Latex allergy
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
8000
Country
Denmark
12. IPD Sharing Statement
Learn more about this trial
Cerebral Responses During Bilateral/Unilateral Sacral Nerve Stimulation for Idiopathic Faecal Incontinence
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