Safety and Efficacy Study of Intrasphincteric Autologous Myoblast Injection to Treat Stress Urinary Incontinence

University Medical Centre Ljubljana

Status and phase

Completed

Phase 2

Phase 1

Conditions

Stress Urinary Incontinence

Treatments

Biological: Transurethral intrasphincteric autologous myoblast implantation

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT01355133

Myoblast/ISD/EKS01

2009-012389-30 (EudraCT Number)

Details and patient eligibility

About

The purpose of this pilot clinical study is to determine if intrasphincteric autologous myoblast injections in combination with electrical stimulation are safe and effective in treating stress urinary incontinence, confirming the optimal dose and assessing tolerability of the procedure.

Enrollment

40 patients

Sex

Female

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Female outpatients, predominant clinical diagnosis of SUI
Have discrete episodes of incontinence (that is, are dry between episodes and not continuously leaking urine, synchronous with increased intra-abdominal pressure from coughing, sneezing, exercising, etc.)
Have a positive Fixed Bladder Volume Cough Stress Test (CST) result; and post void residual volume of <50 ml
Report normal urinary diurnal (≤8/day) and nocturnal (≤2/night) frequency per micturition history
Have had symptoms of SUI for a minimum of 3 months prior to study entry
Can independently use toilet without difficulty
If patients regularly use laxatives, stool softeners, or stool-bulking agents (for example, fibre supplements), the use of these products should remain constant during participation in the study.
Competent to comprehend, sign, and date an Ethics Committee approved informed consent form before any study-specific procedure is performed.
Are women of non-childbearing potential by reason of hysterectomy, other surgery, or natural menopause, or are women of childbearing potential who test negative for pregnancy at the time of enrolment based on a urine pregnancy test and agree to use a medically accepted means of contraception (for example, intrauterine device [IUD], oral or injectable contraceptives, implant, barrier device, sterilization, abstinence, or sex with a vasectomized male partner) for the duration of the study. Women using oral contraceptives or hormone replacement therapy must have a stable dose and regimen for greater than or equal to 3 months prior to entry into the study.

Exclusion criteria

Previous diagnosis of any of the following conditions, disorders, or diseases of the urinary tract:
- Greater than Stage I Anterior (cystocoele), Apical (uteri), or Posterior (rectocoele) Compartment Prolepses as per the POP-Q)
- Ureteric bladder, urethral or rectal fistula
- Uncorrected congenital abnormality leading to urinary incontinence
- Interstitial cystitis
- Urinary urgency that results in leakage (as a predominant symptom)
- Adult enuresis
- Urodynamically proven:
detrusor instability
sensory urgency defined as first sensation of bladder fill (urge to void) of <100 ml; bladder capacity of <300 ml
voiding difficulty
Have no sensation at any time during the simple filling cystometry procedure
Unstable systemic disease including active infection, uncontrolled hypertension, unstable angina, congestive heart failure, or myocardial infarction within 6 months before enrollment
Have a symptomatic urinary tract infection (UTI); or have a history of four or more urinary tract infections in the preceding year.
Have prolonged menstruation (>14 days per month).
Have history of (or currently have) urogenital cancer.
Suffer from severe constipation defined as less than one bowel movement per week
Are pregnant, <12 months postpartum or are lactating
Have had any major inpatient surgery within 3 months prior to study entry
Known infection with human immunodeficiency virus (HIV)
Known active infection with Hepatitis B virus, Hepatitis C virus or Lues.
Any organic or psychiatric disorder that, in the opinion of the investigator, might prevent the subject from completing the study or interfere with the interpretation of the study results.
Have had any anti-incontinence or prolapse surgery, including the following:
- Anterior Repair
- Needle Suspension such as Raz; Pereyra; Stamey; Gittes; and Muzsnai procedures
- Retropubic Procedures: such as Marshall, Marchetti & Krantz; and Burch procedures
- Sling Procedure
- Collagen Injections
- Artificial Sphincter.
Use any of the following:
- Any anti-incontinence device (for example, Reliance, Minigard, or FemAssist) including tampons used to prevent incontinence during participation in the study
- Vaginal pessaries for prolapse or incontinence
- Any nonpharmacologic intervention for incontinence or prolapse (for example, electro stimulation, vaginal cones, or any such device) within the 3 months prior to study entry.
Current use of any of the following drugs: antidepressants, duloxetine, monoamine oxidase inhibitors or other, clonidine, alpha-methyl-DOPA, beta-blockers, guanethidine, reserpine, pentosan polysulfate, or alpha-receptor antagonists/agonists (chronic use).
Current use of any medications for the treatment of urinary incontinence.
Are on a medication regimen including estrogens, anti-estrogens, or diuretics where dose and/or frequency has not been stable for at least the past 12 weeks, or is anticipated to change during the course of the study.
≤ 30 days since receiving an investigational medicinal product or device in another clinical trial. Current enrollment in another clinical trial is not permitted.
Allergy/ intolerance of at least one of the active ingredients or excipients of the investigational products, e.g. bovine protein, gentamycin
Have any abuse disorder within the 5 years prior to study entry; e.g. patients who report regular consumption of >21 alcoholic drinks per week (an average of 3 drinks per day)