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UK Trial of Percutaneous Tibial Nerve Stimulation in Patients With Faecal Incontinence (CONFIDeNT)

Primary Purpose

Faecal Incontinence, Bowel Incontinence

Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Percutaneous Tibial Nerve Stimulation
Sponsored by
Queen Mary University of London
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Faecal Incontinence

Eligibility Criteria

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

Inclusion Criteria:

  • Faecal incontinence sufficiently severe enough to warrant intervention
  • Failure of appropriate conservative therapies
  • Age ≥ 18 years

Exclusion Criteria:

  • Inability to provide informed consent for the research study
  • Inability to fill in the detailed bowel diaries required for outcome assessments (this will exclude participants who do not speak / read English)*
  • Neurological diseases, such as diabetic neuropathy, multiple sclerosis and Parkinson's disease (any participant with painful peripheral neuropathy)
  • Anatomical limitations that would prevent successful placement of needle electrode
  • Other medical conditions precluding stimulation: e.g. bleeding disorders, certain cardiac pacemakers, peripheral vascular disease or ulcer, lower leg cellulitis
  • Congenital anorectal anomalies or absence of native rectum due to surgery
  • A cloacal defect
  • Present evidence of external full thickness rectal prolapse
  • Previous rectal surgery (rectopexy / resection) done < 12 months ago (24 months for cancer),
  • Stoma in situ
  • Chronic bowel diseases such as inflammatory bowel disease leading to chronic uncontrolled diarrhoea
  • Pregnancy or intention to become pregnant
  • Previous experience of SNS or PTNS

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Sham Comparator

    Active Comparator

    Arm Label

    Sham electrical stimulation

    Percutaneous tibial nerve stimulation

    Arm Description

    Sham electrical stimulation to forefoot by TENS

    Active PTNS via Urgent PC Neuromodulation device, Uroplasty

    Outcomes

    Primary Outcome Measures

    Primary outcome: Binary - success or failure based on % patients achieving > or = 50% reduction in faecal incontinence episodes
    From 2 weekly bowel diaries before and after treatment

    Secondary Outcome Measures

    Reduction in faecal incontinence episodes
    Proportion of patients achieving >25%, >75% and 100% reduction in faecal incotinence episodes
    Reduction in Cleveland Clinic Constipation Score

    Full Information

    First Posted
    January 23, 2015
    Last Updated
    January 27, 2015
    Sponsor
    Queen Mary University of London
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02349334
    Brief Title
    UK Trial of Percutaneous Tibial Nerve Stimulation in Patients With Faecal Incontinence
    Acronym
    CONFIDeNT
    Official Title
    CONtrol of Faecal Incontinence Using Distal NeuromodulaTion (CONFIDeNT)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2015
    Overall Recruitment Status
    Completed
    Study Start Date
    January 2012 (undefined)
    Primary Completion Date
    February 2014 (Actual)
    Study Completion Date
    September 2014 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Queen Mary University of London

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Faecal incontinence occurs when a person passes faeces (stools) without the usual control. It is a distressing condition that is actually very common although under-reported because of embarrassment. Milder symptoms may be managed by treatments such as dietary change, drugs and bowel retraining, but many patients still resort to surgery to improve symptoms. Although several operations exist to treat incontinence e.g. those aiming to repair damaged anal sphincter muscles, it is now clear that these often have poor results. Two relatively new treatments called sacral nerve stimulation (SNS) and percutaneous tibial nerve stimulation (PTNS) involve sending pulses of electricity to the nerves controlling the bowel and muscles of the anus (anal sphincter). SNS does this by inserting electrodes in the lower back just above the tailbone and connecting them to an implanted electrical stimulator which is buried in the buttock and acts a bit like a heart pacemaker. SNS is a relatively well-established treatment in specialist centres, which has been used for over 10 years. It has been shown in studies to be successful for faecal incontinence achieving some improvement in at least three quarters of patients. In Europe, this procedure is fast becoming first treatment offered when non-surgical treatments fail. Nevertheless, SNS is not a miracle cure for all, requiring 2 operations, with potential complications and expensive equipment (> £10,000 approx). PTNS is a newer treatment, which involves electrically stimulating a nerve at the ankle, using a very small needle, as an outpatient (a bit like acupuncture). This sends signals back to the spine region to try and improve symptoms of faecal incontinence. Since this is a newer treatment, fewer studies have been performed to quantify how successful it is, but early results of PTNS suggest that it may be as good as SNS. If this is true, this is very important because it is much less invasive and considerably cheaper than SNS (equipment £500 per patient). This project will for the first time determine how effective PTNS is in the treatment of patients with faecal incontinence, by comparing it to sham (fake stimulation). This study is a properly designed clinical trial of 212 patients in at least 14 UK Specialist Centres.. The results of this trial will lead to direct benefits for patients and the NHS.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Faecal Incontinence, Bowel Incontinence

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    227 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Sham electrical stimulation
    Arm Type
    Sham Comparator
    Arm Description
    Sham electrical stimulation to forefoot by TENS
    Arm Title
    Percutaneous tibial nerve stimulation
    Arm Type
    Active Comparator
    Arm Description
    Active PTNS via Urgent PC Neuromodulation device, Uroplasty
    Intervention Type
    Device
    Intervention Name(s)
    Percutaneous Tibial Nerve Stimulation
    Primary Outcome Measure Information:
    Title
    Primary outcome: Binary - success or failure based on % patients achieving > or = 50% reduction in faecal incontinence episodes
    Description
    From 2 weekly bowel diaries before and after treatment
    Time Frame
    3 months
    Secondary Outcome Measure Information:
    Title
    Reduction in faecal incontinence episodes
    Time Frame
    3 months
    Title
    Proportion of patients achieving >25%, >75% and 100% reduction in faecal incotinence episodes
    Time Frame
    3 months
    Title
    Reduction in Cleveland Clinic Constipation Score
    Time Frame
    3 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Faecal incontinence sufficiently severe enough to warrant intervention Failure of appropriate conservative therapies Age ≥ 18 years Exclusion Criteria: Inability to provide informed consent for the research study Inability to fill in the detailed bowel diaries required for outcome assessments (this will exclude participants who do not speak / read English)* Neurological diseases, such as diabetic neuropathy, multiple sclerosis and Parkinson's disease (any participant with painful peripheral neuropathy) Anatomical limitations that would prevent successful placement of needle electrode Other medical conditions precluding stimulation: e.g. bleeding disorders, certain cardiac pacemakers, peripheral vascular disease or ulcer, lower leg cellulitis Congenital anorectal anomalies or absence of native rectum due to surgery A cloacal defect Present evidence of external full thickness rectal prolapse Previous rectal surgery (rectopexy / resection) done < 12 months ago (24 months for cancer), Stoma in situ Chronic bowel diseases such as inflammatory bowel disease leading to chronic uncontrolled diarrhoea Pregnancy or intention to become pregnant Previous experience of SNS or PTNS

    12. IPD Sharing Statement

    Learn more about this trial

    UK Trial of Percutaneous Tibial Nerve Stimulation in Patients With Faecal Incontinence

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