Percutaneous Tibial Nerve Stimulation for the Treatment of Fecal Incontinence (TENSIA)
Primary Purpose
Fecal Incontinence
Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
active stimulation
sham stimulation
Sponsored by
About this trial
This is an interventional treatment trial for Fecal Incontinence focused on measuring fecal incontinence
Eligibility Criteria
Inclusion Criteria:
- fecal incontinence, refractory to medical treatment,for more than 3 months,with at least one episode of anal incontinence and/or urgency per month
- patient with no knowledge of cutaneous stimulation
- patients with NHS
Exclusion Criteria:
- older than 18 years old
- pregnancy
- implanted stimulator
- cutaneous lesion
- cutaneous anesthesia
- patients without oral contraception
- Guardianship and curatorship
- fecal incontinence secondary to anorectal malformation, surgical sequelae, significative sphincteric lesion leading to repair at a first time, rectal prolapse, active neurological disease
- patient already treated by sacral nerve stimulation or stimulated graciloplasty, artificial bowel sphincter, radiofrequency
Sites / Locations
- Leroi
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Sham Comparator
Arm Label
Active stimulation
sham stimulation
Arm Description
Percutaneous posterior tibial nerve stimulation
Inefficient percutaneous posterior tibial nerve stimulation
Outcomes
Primary Outcome Measures
fecal incontinence episode per week
Secondary Outcome Measures
cleveland clinic score FIQL score analogic visual scale urinary score and anorectal manometry
Full Information
NCT ID
NCT00977652
First Posted
September 15, 2009
Last Updated
August 22, 2011
Sponsor
University Hospital, Rouen
Collaborators
Ministry of Health, France
1. Study Identification
Unique Protocol Identification Number
NCT00977652
Brief Title
Percutaneous Tibial Nerve Stimulation for the Treatment of Fecal Incontinence
Acronym
TENSIA
Official Title
Short Term Efficacy of Percutaneous Tibial Nerve Stimulation for the Treatment of Fecal Incontinence:Randomized Controlled Study
Study Type
Interventional
2. Study Status
Record Verification Date
August 2011
Overall Recruitment Status
Completed
Study Start Date
October 2009 (undefined)
Primary Completion Date
June 2011 (Actual)
Study Completion Date
June 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital, Rouen
Collaborators
Ministry of Health, France
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Fecal incontinence is a major public health issue since 10% of the French population aged 45 has to deal with it. Different treatments exist and have already been evaluated, like the sacral nerve stimulation (SNS) which has proved to be efficient in 75 to 100% of the anal incontinence patients without significant sphincteric lesions or rectal prolapse. However, the treatment is expensive and can have side effects. Moreover, about 20 to 30% of the patients can develop a resistance to the SNS only a few months following the definite implantation. Yet the development of the posterior tibial nerve stimulation (PNTS) offers a new perspective. It consists in stimulating the same metameric area as the sacral nerves. It is regularly used for the treatment of urinary incontinence caused by overactive bladder. It is a non-invasive technique, causing but a few side effects. A preliminary study showed that 7 in 10 incontinent patients saw an improvement when treated with PTNS.
Purpose:
The aim of this study is to analyse and evaluate the PTNS technique in the short term as a treatment of anal incontinence. It is done through the means of a multi-centric prospective randomized study.
Patients:
Will be included: all patients followed for anal incontinence (either with liquid or solid stools) having at least one accident a month for 3months, and who are not diagnosed with colorectal lesions and who are without anal or rectal significant anatomic anomalies, without rectal prolapse, and who have failed to respond to medical treatment (such as medicine or perineal reeducation). The main criterium to analyze the efficiency will be the number of fecal incontinence episodes on a bowel diary. The investigators aim to incorporate 144 patients, that is 72 in each group. 12 centers will take part in this study, that will last 2 years and 3 months. They are the centers of: Bordeaux, Clermont-Ferrand, Grenoble, Lyon, Marseille, Nancy, Nantes, Paris, Diaconesses-Croix,Paris Rothschild, Rennes, Rouen, and Toulouse.
Method:
The PTNS consists in setting two electrodes on the posterial tibial nerve pathway. The electrodes are connected to an external stimulator. After having drawn lots, patients will be treated for 3months either with effective stimulation (frequency: 14hz; impulse duration: 210usec;intensity:sensibility threshold), or with shame stimulation (intensity: 0mAmp). There will be two daily sessions of stimulation (effective, or shame), 20 min each. A pre-treatment assessment will be established, composed of a stool diary, a Cleveland Clinic score, a Fecal Incontinence Quality of Life scale and an anorectal manomety, that will all be repeated by the end of the treatment.
Expected Results:
The investigators hope to prove the short term efficacy of the PTNS on anal incontinence patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fecal Incontinence
Keywords
fecal incontinence
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
144 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Active stimulation
Arm Type
Active Comparator
Arm Description
Percutaneous posterior tibial nerve stimulation
Arm Title
sham stimulation
Arm Type
Sham Comparator
Arm Description
Inefficient percutaneous posterior tibial nerve stimulation
Intervention Type
Procedure
Intervention Name(s)
active stimulation
Intervention Description
percutaneous posterior tibial nerve stimulation with following parameters: frequency: 14hz; impulse duration: 210usec;intensity:sensibility threshold during 3 months
Intervention Type
Procedure
Intervention Name(s)
sham stimulation
Intervention Description
Same location with the same device than active stimulation but amplitude of stimulation = 0
Primary Outcome Measure Information:
Title
fecal incontinence episode per week
Time Frame
three months
Secondary Outcome Measure Information:
Title
cleveland clinic score FIQL score analogic visual scale urinary score and anorectal manometry
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
fecal incontinence, refractory to medical treatment,for more than 3 months,with at least one episode of anal incontinence and/or urgency per month
patient with no knowledge of cutaneous stimulation
patients with NHS
Exclusion Criteria:
older than 18 years old
pregnancy
implanted stimulator
cutaneous lesion
cutaneous anesthesia
patients without oral contraception
Guardianship and curatorship
fecal incontinence secondary to anorectal malformation, surgical sequelae, significative sphincteric lesion leading to repair at a first time, rectal prolapse, active neurological disease
patient already treated by sacral nerve stimulation or stimulated graciloplasty, artificial bowel sphincter, radiofrequency
Facility Information:
Facility Name
Leroi
City
Rouen
ZIP/Postal Code
76000
Country
France
12. IPD Sharing Statement
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Percutaneous Tibial Nerve Stimulation for the Treatment of Fecal Incontinence
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