UK Trial of Percutaneous Tibial Nerve Stimulation in Patients With Faecal Incontinence
NCT ID: NCT02349334
Last Updated: 2015-01-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
PHASE3
227 participants
INTERVENTIONAL
2012-01-31
2014-09-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Tibial Nerve Stimulation for Faecal Incontinence
NCT00530933
Percutaneous Tibial Nerve Stimulation in the Treatment of Fecal Incontinence
NCT00974909
Tibial Nerve Stimulation in Combination With Biofeedback
NCT02888899
Optimising Treatments for Faecal Incontinence
NCT04273009
Prospective, Multicenter Trial to Investigate the Safety and Efficacy of Percutaneous Tibial Nerve Stimulation for the Treatment of Fecal Incontinence
NCT01666405
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Sham electrical stimulation
Sham electrical stimulation to forefoot by TENS
Percutaneous Tibial Nerve Stimulation
Percutaneous tibial nerve stimulation
Active PTNS via Urgent PC Neuromodulation device, Uroplasty
Percutaneous Tibial Nerve Stimulation
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Percutaneous Tibial Nerve Stimulation
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Failure of appropriate conservative therapies
* Age ≥ 18 years
Exclusion Criteria
* 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
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Queen Mary University of London
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
09/104/16
Identifier Type: OTHER_GRANT
Identifier Source: secondary_id
34825
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.