Fecal Incontinence Clinical Trial
Official title:
Prospective Randomised Placebo Controlled Study Into Percutaneous and Transcutaneous Tibial Nerve Stimulation for Faecal Incontinence
The purpose of this study is to determine whether tibial nerve stimulation is an effective treatment for faecal incontinence.
Status | Recruiting |
Enrollment | 66 |
Est. completion date | April 2009 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Over 18 - Incontinence to solid or liquid faeces Exclusion Criteria: - Previous congenital or acquired spinal injury, spinal tumour or spinal surgery - Neurological diseases, such as diabetic neuropathy, multiple sclerosis and Parkinson's disease - Peripheral vascular disease - Diabetes mellitus - Congenital anorectal malformations - Previous rectal surgery (rectopexy / resection) done < 12 months ago (24 months for cancer) - Present evidence of external full thickness rectal prolapse - Chronic bowel diseases such as inflammatory bowel disease - Chronic diarrhoea, uncontrolled by drugs or diet - Anatomical limitations that would prevent successful placement of an electrode - Previous use of transcutaneous electrical nerve stimulation Stoma in situ |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United Kingdom | St Mark's Hospital | London |
Lead Sponsor | Collaborator |
---|---|
London North West Healthcare NHS Trust | Uroplasty, Inc |
United Kingdom,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The difference in the percentage of patients with a 20% reduction in episodes of faecal incontinence between the placebo and treatment groups. | 14 weeks | ||
Secondary | The difference in the improvements in the St Mark's incontinence score, quality of life scales, and physiological parameters between the treatment and placebo groups. | 14 weeks | ||
Secondary | The difference in the improvements in the urinary symptoms between placebo and treatment groups. | 14 weeks |
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