Status:
UNKNOWN
Trial Evaluating Transvaginal Electrical Stimulation With a Home Use Programmable Device for Urinary Stress Incontinence
Lead Sponsor:
Akontis
Conditions:
Urinary Stress Incontinence
Eligibility:
FEMALE
18+ years
Phase:
PHASE2
Brief Summary
To compare the effectiveness of a transvaginal electrical stimulation by a home use programmable device to a placebo device for urinary incontinence in women
Eligibility Criteria
Inclusion
- \>=18 years old
- Signed informed consent form
- Women with urinary stress incontinence defined as follow
- Involuntary loss of urine during increased abdominal pressure. In case of mix urinary incontinence (i.e., stress urinary incontinence associated to urge urinary incontinence) the discomfort related to stress incontinence as evaluated on a 0 (no discomfort) to 100 (maximum discomfort) visual analogic scale is higher for stress incontinence than for urge incontinence symptoms.
- closure pressure between 10 and 60 cm H2O
- the discomfort related to stress incontinence as evaluated on a 0 (no discomfort) to 100 (maximum discomfort) visual analogical scale is higher than 40/100
- Patients never treated with transvaginal electrical stimulation
- Vaginal muscle strength less than 3/5 on the muscular testing
- Positive Pad test (\>2 g of leakage measure by pad test with standardised bladder volume)
Exclusion
- Patient refusing to sign the consent form
- patient unable to understand or follow the protocol
- inadequate cognitive ability
- patient participating in another research protocol within the 3 previous months
- pregnancy
- women with no contraception
- pacemaker
- history of recent (\< 1 year) transvaginal electrical stimulation treatment at home
- urinary incontinence other than stress incontinence
- neurological disease
- permanent metrorrhagia
- ongoing urinary tract infections
- vaginal prolapse \> 2
- untreated atrophic vaginitis
- history of surgical treatment for urinary stress incontinence or genital prolapse
- recent pelvic surgery (\<6 months)
- anatomic defect that preclude the use of the device
- genitourinary cancer or colic cancer
- patient already treated for urinary stress incontinence
- Recent oestrogen treatment (less than 3 weeks)
Key Trial Info
Start Date :
January 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 1 2008
Estimated Enrollment :
150 Patients enrolled
Trial Details
Trial ID
NCT00762593
Start Date
January 1 2006
End Date
October 1 2008
Last Update
October 17 2008
Active Locations (1)
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1
Centre européen d'explorations gynécologiques
Paris, France, 75005