Comparison of Sacral Nerve Modulation and Pudendal Nerve Stimulation in Treatment of Fecal Incontinence
Primary Purpose
Fecal Incontinence
Status
Completed
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Sacral nerve modulation
Pudendal nerve stimulation
Sponsored by
About this trial
This is an interventional treatment trial for Fecal Incontinence focused on measuring Fecal Incontinence, Colorectal surgery, Sacral nerve stimulation, Pudendal nerve stimulation
Eligibility Criteria
Inclusion Criteria:
- fecal incontinence nonresponsive to conservative treatment
Exclusion Criteria:
- sacral or perineal infection
- sphincter defect larger than 60° (sonography)
- pregnancy
Sites / Locations
- Department of Surgey, Cantonal Hospital St. Gallen
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Sacral nerve modulation first
Pudendal nerve stimulation first
Arm Description
Sacral nerve modulation is applied before the pudendal nerve stimulation. There is no "wash-out" period (pause) between the two treatments.
Pudendal nerve stimulation is applied before the sacral nerve modulation. There is no "wash-out" period (pause) between the two treatments.
Outcomes
Primary Outcome Measures
Power consumption of stimulator
Secondary Outcome Measures
Wexner Score (Jorge 1993)
Incidence of surgical complications (adverse events) graded according to Dindo (2004)
Quality of Life (FIQL (Rockwood 2000))
Full Information
NCT ID
NCT01069016
First Posted
February 11, 2010
Last Updated
July 20, 2017
Sponsor
Cantonal Hospital of St. Gallen
1. Study Identification
Unique Protocol Identification Number
NCT01069016
Brief Title
Comparison of Sacral Nerve Modulation and Pudendal Nerve Stimulation in Treatment of Fecal Incontinence
Official Title
Comparison of Sacral Nerve Modulation and Pudendal Nerve Stimulation in Treatment of Fecal Incontinence
Study Type
Interventional
2. Study Status
Record Verification Date
July 2017
Overall Recruitment Status
Completed
Study Start Date
February 2010 (Actual)
Primary Completion Date
July 2014 (Actual)
Study Completion Date
February 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cantonal Hospital of St. Gallen
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Sacral nerve modulation (SNM) is an established treatment for refractory lower urinary tract and bowel dysfunction (Spinelli 2008). Pudendal nerve stimulation (PNS) has been proposed for patients failing SNM treatment of urinary dysfunction (Spinelli 2005). In this study SNM and PNS are compared for the treatment of fecal incontinence. In a test phase, both treatments will be applied for one week each in a randomized and blinded order (cross-over design). After the test phase the more successful treatment will be determined and applied permanently. If both treatments are equally sufficient, PNS will be chosen for permanent stimulation, since preliminary data indicate that PNS has a lower power consumption than SNM. Lower power consumption results in a longer lifetime of the stimulator, thus requiring less replacement surgeries.
Detailed Description
Primary Surgery:
Implantation of two electrodes, one placed next to the sacral nerve, one close to the pudendal nerve. Electrode wires are passed through the skin just above the gluteal region and are marked S and P. One of the sub-investigators (not involved in the follow-up) replaces the S and P marks by 1 and 2 marks in absence of the operating surgeon. Assignment of 1 and 2 is carried out in a predefined randomized fashion (computerized block randomization).
Test phase:
Electrode labeled 1 is connected to a stimulator and the nerve is stimulated for one week, then the other electrode is stimulated for a week.
Based on bowel habit diary, Wexner score (Jorge 1993) and subjective experience of the patient, the more successful treatment is chosen. If both electrodes were equally successful, the pudendal nerve electrode will be chosen for permanent stimulation.
Secondary surgery:
After unblinding, the less effective electrode is removed and the remaining electrode is connected to an implanted stimulator (permanent phase). In case both treatments were unsuccessful, both electrodes are removed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fecal Incontinence
Keywords
Fecal Incontinence, Colorectal surgery, Sacral nerve stimulation, Pudendal nerve stimulation
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Sacral nerve modulation first
Arm Type
Experimental
Arm Description
Sacral nerve modulation is applied before the pudendal nerve stimulation. There is no "wash-out" period (pause) between the two treatments.
Arm Title
Pudendal nerve stimulation first
Arm Type
Experimental
Arm Description
Pudendal nerve stimulation is applied before the sacral nerve modulation. There is no "wash-out" period (pause) between the two treatments.
Intervention Type
Procedure
Intervention Name(s)
Sacral nerve modulation
Other Intervention Name(s)
SNM, Sacral nerve stimulation, SNS
Intervention Description
For one week the sacral nerve is continuously stimulated by an external pulse generator. Strength of stimulation can be adjusted by the patient.
Intervention Type
Procedure
Intervention Name(s)
Pudendal nerve stimulation
Other Intervention Name(s)
PNS
Intervention Description
For one week the pudendal nerve is continuously stimulated by an external pulse generator. Strength of stimulation can be adjusted by the patient.
Primary Outcome Measure Information:
Title
Power consumption of stimulator
Time Frame
14 days
Secondary Outcome Measure Information:
Title
Wexner Score (Jorge 1993)
Time Frame
7, 14 days, 3, 6 & 12 months
Title
Incidence of surgical complications (adverse events) graded according to Dindo (2004)
Time Frame
30 days
Title
Quality of Life (FIQL (Rockwood 2000))
Time Frame
14 days, 3, 6 & 12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
fecal incontinence nonresponsive to conservative treatment
Exclusion Criteria:
sacral or perineal infection
sphincter defect larger than 60° (sonography)
pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lukas Marti, MD
Organizational Affiliation
Dep. of Surgery, Cantonal Hospital St. Gallen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Surgey, Cantonal Hospital St. Gallen
City
St.Gallen
ZIP/Postal Code
9007
Country
Switzerland
12. IPD Sharing Statement
Citations:
PubMed Identifier
18336992
Citation
Spinelli M, Sievert KD. Latest technologic and surgical developments in using InterStim Therapy for sacral neuromodulation: impact on treatment success and safety. Eur Urol. 2008 Dec;54(6):1287-96. doi: 10.1016/j.eururo.2008.01.076. Epub 2008 Feb 8.
Results Reference
background
PubMed Identifier
15977260
Citation
Spinelli M, Malaguti S, Giardiello G, Lazzeri M, Tarantola J, Van Den Hombergh U. A new minimally invasive procedure for pudendal nerve stimulation to treat neurogenic bladder: description of the method and preliminary data. Neurourol Urodyn. 2005;24(4):305-9. doi: 10.1002/nau.20118.
Results Reference
background
PubMed Identifier
8416784
Citation
Jorge JM, Wexner SD. Etiology and management of fecal incontinence. Dis Colon Rectum. 1993 Jan;36(1):77-97. doi: 10.1007/BF02050307.
Results Reference
background
PubMed Identifier
10813117
Citation
Rockwood TH, Church JM, Fleshman JW, Kane RL, Mavrantonis C, Thorson AG, Wexner SD, Bliss D, Lowry AC. Fecal Incontinence Quality of Life Scale: quality of life instrument for patients with fecal incontinence. Dis Colon Rectum. 2000 Jan;43(1):9-16; discussion 16-7. doi: 10.1007/BF02237236.
Results Reference
background
PubMed Identifier
15273542
Citation
Dindo D, Demartines N, Clavien PA. Classification of surgical complications: a new proposal with evaluation in a cohort of 6336 patients and results of a survey. Ann Surg. 2004 Aug;240(2):205-13. doi: 10.1097/01.sla.0000133083.54934.ae.
Results Reference
background
Links:
URL
http://www.chirurgie.kssg.ch/home/unsere_klinik/Leistungsangebot_standort_st_gallen/koloproktologie.html
Description
Proctological consultations, Department of Surgery
Learn more about this trial
Comparison of Sacral Nerve Modulation and Pudendal Nerve Stimulation in Treatment of Fecal Incontinence
We'll reach out to this number within 24 hrs