Urinary Incontinence, Stress Urinary Incontinence, Urge Incontinence
Conditions
Brief summary
This multi-center clinical trial will evaluate the safety and long-term efficacy of hybrid fractional 2940 nm and 1470 lasers for improvement of symptoms of urinary incontinence.
Detailed description
Both 2940 nm Er:YAG (Erbium-doped yttrium aluminium garnet) and 1470 nm diode lasers are cleared by the Food and Drug Administration (FDA) for ablation, vaporization, coagulation of soft tissue and for skin resurfacing. Fractional delivery of laser is a well-established method that stimulates tissue remodeling in the dermis while leaving the surrounding tissue intact in order to decrease healing time. The layers of skin and vaginal mucosal tissue exhibit similarities that suggest the clinical results seen with skin resurfacing may be translated to the vaginal tissue. Improved vaginal tissue tone and increased collagen formation in the lamina propria beneath the urethra may lead to improved urinary control. This multi-centered, 18-month prospective clinical trial will determine the safety and long-term effectiveness of hybrid fractional 2940 nm and 1470 nm lasers (Hybrid Fractional Laser) as an alternative non-surgical, non-hormonal treatment for improvement of symptoms of urinary incontinence.
Interventions
DEVICEHybrid Fractional Laser
Consecutive and coincident fractional 2940 nm and 1470 nm lasers
Sponsors
Sciton
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
30 Years to 75 Years
Healthy volunteers
Yes
Inclusion criteria
1. Healthy biological female aged between 30 to 75 years 2. Is experiencing at least one or a combination of the following symptoms of urinary incontinence (UI) 1. involuntary urine leakage on effort, exertion, sneezing, coughing 2. sudden intense urge to urinate followed by involuntary loss of urine 3. Has been experiencing symptoms of UI for greater than 3 months 4. Normal urinalysis 5. Has indicated willingness to participate in the study by signing an informed consent form 6. Can read, understand and sign informed consent form 7. Agree to adhere to the treatment and follow-up schedule and post treatment care instructions
Exclusion criteria
1. Undiagnosed abnormal genital bleeding 2. Has history of pelvic surgery or other energy-based vaginal therapy within 6 months prior to enrollment 3. Is pregnant or planning to get pregnant within the study period 4. Is currently breastfeeding 5. Has an active sexually transmitted infection (STI) 6. Has equal to or greater than stage III prolapse, according to pelvic organ prolapse quantification system (POP-Q test) 7. Has signs or symptoms of vaginitis/vulvitis 8. Has signs or symptoms of acute urinary tract infection (UTI) 9. Has voiding dysfunction or urinary retention 10. Has predominantly overactive bladder (OAB) as proven by urodynamics 11. Is currently taking medication for treating urinary incontinence 12. Has a known history of neurologic disease 13. Has history of heart failure 14. Any medical conditions that might interfere with wound healing 15. Has history of abnormal wound healing 16. Has participated in any clinical trial involving an investigational drug or procedure within past 30 days 17. The investigator feels that for any reason the subject is not eligible to participate in the study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change from baseline in Cough Stress Test | 14 months | A diagnostic test to simulate accidental release of urine when the patient coughs. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change from baseline in Urogenital Distress Inventory (UDI-6) | 14 months | A 6-item self-report instrument that assesses symptom distress and the impact on daily life of urinary incontinence. |
| Change from baseline in Female Sexual Function Index (FSFI) | 14 months | A multidimensional self-report instrument for assessment of female sexual function. |
| Change from baseline in Incontinence Impact Questionnaire (IIQ-7) | 14 months | A 7-item self-report instrument designed to assess the impact of urinary incontinence on a patient's life. |
| Change from baseline in Urodynamic Testing | 14 months | Quantitative measures of uroflowmetry, post-void residual (PVR) urine, cystometry, leak-point pressure, pressure flow, urethral pressure profile, and the functional urethral length. |
| Incidence and severity of treatment-related Adverse Events | 14 months | Incidence and severity of treatment-related adverse events (i.e. pain, edema, erythema, altered sensation, scarring, and/or potential infection). |
| Change from baseline in Histology | 14 months | Change from baseline in epithelial thickness, collagen, elastin, vascularity, and fibroblast density. |
Countries
United States
Outcome results
None listed