Stress Urinary Incontinence
Conditions
Keywords
SUI, Incontinence, Laser, High Intensity Tesla Magnetic Stimulation
Brief summary
To investigate the efficacy of combined laser and HITS treatment for female stress urinary incontinence (SUI)
Detailed description
This study is a single-centre, two-arm randomized control trial study conducted according to Helsinki Declaration. Women with symptoms of stress urinary incontinence (SUI) (stress or mixed with stress incontinence as the predominant symptom) will be enrolled. The efficacy and safety of combined treatment with non-ablative intravaginal Er:YAG laser procedure and high intensity Tesla magnetic stimulation will be compared to the treatment of non-ablative intravaginal Er:YAG laser alone.
Interventions
DEVICElaser and High intensity Tesla magnetic stimulation
Three (3) non-ablative Er:YAG laser treatments will be applied at monthly intervals followed by Eight (8) HITS therapies) Patients will receive two (2) HITS treatments per week for four (4) weeks(.
DEVICElaser (without HITS treatment)
Three (3) non-ablative Er:YAG laser treatments will be applied at monthly intervals as described above.
Sponsors
Fotona d.o.o.
Cork University Maternity Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
a two-arm parallel assignment, randomized control trial
Eligibility
Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
1. Adult female, 18 years of age or older 2. Clinical diagnosis of stress or mixed urinary incontinence, with stress incontinence as the predominant symptom (SUI or MUI)
Exclusion criteria
1. Very severe urinary incontinence (International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form (ICIQ-UI SF) ICIQ-UI )score at baseline \>18 or Pad test \> 50 gr) 2. Pregnancy 3. BMI\>35 4. Acute urinary tract infections (UTIs) 5. History of a genital fistula, a thin recto-vaginal septum as determined by the investigator or history of a fourth-degree laceration during screening physical exam (e.g., perineal body) 6. Active sexually transmitted disease upon vaginal exam (as determined by the investigator) that precludes treatment or any other vaginal infection 7. Prolapse grade 2 or higher 8. History of radiotherapy for cervical or uterine cancer 9. Medical condition that may interfere with participants' compliance to the protocol 10. Medical condition for which the HITS and laser therapy are contraindicated 11. Previous laser or HITS treatment for SUI
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Symptoms of stress urinary incontinence | measured at 3 and 6 months | Change of symptoms of stress and/or mixed urinary incontinence as measured by change in one hour pad test (gr/h) results at the end of treatment period from the baseline results. |
| Adverse events | up to 6 month post procedure | The number and severity of treatment-related Adverse Events. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| PGI-I - Patient Global Impression of Improvement | measured at 3 and 6 months | The Patient Global Impression of Improvement (PGI-I) is a global index that may be used to rate the response of a condition to a therapy (transition scale). It is a simple, direct, easy to use scale that is intuitively understandable to clinicians. 1-7: Very much better- 1, Much better -2, A little better-3, No change-4, A little worse-5, Much worse-6, Very much worse-7. |
| QUID - Questionnaire for Urinary Incontinence Diagnosis | measured at 3 and 6 months | The Questionnaire for Urinary Incontinence Diagnosis (QUID) identifies the presence and frequency of stress and urge incontinence symptoms. Three items focus on stress incontinence symptoms and three on urge incontinence symptoms. Each item includes 6 frequency-based response options, ranging from none of the time to all of the time, which are scored from 0 to 5 points. Scores are calculated in an additive fashion, resulting in separate Stress and Urge scores, each ranging from 0 to 15 points. |
| International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form (ICIQ-UI SF) | measured at 3 and 6 months | The ICIQ-UI Short Form is a questionnaire for evaluating the frequency, severity and impact on quality of life (QoL) of urinary incontinence in men and women in research and clinical practice across the world. This short and simple questionnaire is also of use to general practitioners and clinicians in both primary and secondary care institutions to screen for incontinence, to obtain a brief yet comprehensive summary of the level, impact and perceived cause of symptoms of incontinence and to facilitate patient-clinician discussions. Scoring is between 0 to 21 (worse symptoms ) |
| One-hour pad test. | measured at 3 and 6 months | he testing protocol has been standardized by International Continence Society (ICS-pad test): * the test is started by putting one pre-weighted pad without patient voiding, * patient drinks 500 ml of sodium-free liquid in \<15 min- then sits or rests, * patient walks for 30 min, including climbing one flight of stairs (up and down), * patient performs the following activities: standing up from sitting (10x), coughing vigorously (10x), running on the spot for 1 min, bending to pick up an object from the floor (5x), and washing hands in running water for 1min (this activity program may be modified according to the patient's physical fitness), * the total amount of urine leaked is determined by weighing the pad. If a moderately full bladder cannot be maintained through the hour (if the patient must void), the test has to be started again. |
| FSFI - The Female Sexual Function Index | measured at 3 and 6 months | FSFI - The Female Sexual Function Index is a generalized questionnaire utilized to assess sexual function in women in a general population. It has been validated on clinically diagnosed samples of women with female sexual arousal disorder, female orgasmic disorder, and hypoactive sexual desire disorder. Scoring is between 2 (low sexual function)-36 (high sexual function). |
Contacts
Primary ContactYair Daykan, M.D
Backup ContactSuzan Wilson, M.D
Outcome results
None listed