Stress Urinary Incontinence, Urinary Incontinence
Conditions
Keywords
incontinence, urinary incontinence, stress urinary incontinence, platelet rich plasma, PRP,, outpatient treatment, nonsurgical treatment
Brief summary
Stress urinary incontinence (SUI) is defined as involuntary loss of urine on effort or physical exertion or on sneezing or coughing. Platelet-rich plasma (PRP) is an autologous solution of human plasma containing various growth factors witch enhance regeneration and healing process. The aim of this study is to evaluate the efficacy and safety of PRP in the treatment of the female SUI.
Interventions
BIOLOGICALPlatelet Rich Plasma Injections
PRP injected into 9 sites of the distal anterior one-third of the vagina using a small 30-gauge needle. The injections were performed at 10, 12 and 2 o'clock in 3 different levels of the urethra 1-2 cm apart (distal, mid and proximal). The participants will receive 2 PRP injections at 4-6-week intervals. Xylocaine gel 2% is applied to the distal anterior vaginal wall 20 minutes before injections.
OTHERNormal Saline Injections
Normal saline injected into 9 sites of the distal anterior one-third of the vagina using a small 30-gauge needle. The injections were performed at 10, 12 and 2 o'clock in 3 different levels of the urethra 1-2 cm apart (distal, mid and proximal). The participants will receive 2 injections at 4-6-week intervals.
Sponsors
National and Kapodistrian University of Athens
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Adult women with stress urinary incontinence
Exclusion criteria
* pregnancy, * history of active malignant pathology, * mental disorders making them unable to give consent, * undiagnosed abnormal uterine bleeding, * genitourinary fistula, * anti-incontinence surgery, * pelvic organ prolapse stage \> 2 according to POP-Q system
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Stress urinary incontinence symptoms | 6-12 months | International Consultation on Incontinence Questionnaire Female Lower Urinary Tract Symptoms Modules (ICIQ-FLUTS) Number of items: 12 Question items: Nocturia,Urgency, Bladder pain, Frequency, Hesitancy, Straining, Intermittency, Urge urinary incontinence, Frequency of urinary incontinence, Stress urinary incontinence, Unexplained urinary incontinence, Nocturnal enuresis Completion time: 4-5 minutes Scoring: 0-16 filling symptoms subscale 0-12 voiding symptoms subscale 0-20 incontinence symptoms subscale 0-48 where all subscale scores are added. Bother scales are not incorporated in the overall score but indicate impact of individual symptoms for the patient Higher scores indicate greater impact of individual symptoms for the patient. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Impact of urinary incontinence on the quality of life | 6-12 months | King's Health Questionnaire (KHQ) Description: The KHQ is an assessment of health-related quality of life related to a specific condition. Format: 21 items about urinary tract symptoms yield scores in 9 domains (general health perception, incontinence impact, role limitations, physical limitations, social limitations, personal relationships, emotions, sleep/energy & severity of symptoms). Scoring: Each item is rated using a 4 or 5 points likert scale. Domain scores range from 0 (best) to 100 (worst). There are 2 single-item domains (general health perceptions, and incontinence impact) and the severity of symptoms domain is scored using a scale from 0 (best) to 30 (worst). |
| Assessment of urine loss (1-hr pad test) | 6-12 months | One-hour pad test standardized by International Continence Society (ICS): * started by putting one pre-weighted pad, * patient drinks 500 ml in \<15 min- then sits or rests, * patient walks for 30 min, * patient performs the following activities: standing up from sitting, coughing vigorously, running on the spot for 1 min, bending to pick up an object from the floor, and washing hands in running water for 1min * the total amount of urine leaked is determined by weighing the pad. Interpretation: The upper limit of weight increase for the 1-hr test in continent women is 1.4 grams. A weight gain of less than 1.4 g during 1-hr test could be a result of sweating or vaginal discharge. An increase of 1-10 g is classified as representing mild incontinence, 11-50 g moderate and \>50 g severe incontinence. |
| Level of discomfort during injections (VAS score) | 6-12 months | The visual analog scale (VAS) is pain rating scale. Scores are based on self-reported measures of symptoms that are recorded with a single handwritten mark placed at one point along the length of a 10-cm line that represents a continuum between the two ends of the scale-no pain on the left end (0 cm) of the scale and the worst pain on the right end of the scale (10 cm). |
| Patient Global Impression of Improvement | 6-12 months | The Patient Global Impression of Improvement (PGI-I) is a validated generic tool for assessment of the over-all improvement or deterioration that the patient may experience following the treatment. The PGI-I is a transition scale that is a single question asking the patient to rate their urinary tract condition now, as compared with how it was prior to before beginning treatment on a scale from 1. Very much better to 7. Very much worse. Therefore, lower values correlate with increased satisfaction. |
Countries
Greece
Contacts
Primary ContactStavros Athanasiou, Professor
Outcome results
None listed