BridgeMD
New treatment option for Overactive Bladder
Official title A Real World Study of eCoin for Urgency Urinary Incontinence: Post Approval Evaluation (RECIPE)
ClinicalTrials.gov ID: NCT05685433
What this study is testing
- What it's testing
- A prospective, multicenter, single-arm study to evaluate the safety and effectiveness of the eCoin® implanted tibial nerve stimulator in subjects with urgency urinary incontinence (UUI).
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- Women and men above 18 years old with gender percentages reflective of disease prevalence in the U.S. population
- Individual with diagnosis of overactive bladder with urgency urinary incontinence.
- Individual has at least one urgency urinary incontinence episode on each of three days as determined on a 3-day voiding diary.
- Individual gives written informed consent.
- Individual is mentally competent and able to understand all study requirements.
You likely can't join if
- Individual is not appropriate for eCoin therapy based upon the US FDA-approved IFU requirements.
- Individual has clinically significant bladder outlet obstruction. (Suspected bladder outlet obstruction will be initially assessed by uroflow study...
- Individual has predominantly stress urinary incontinence (greater than 1/3 of leaks on baseline diary are stress).
- Individual has an active urinary tract infection at time of enrollment.
- Individual has known polyuria.
- Individual has significant lower urinary tract pain or has been diagnosed with interstitial cystitis or bladder pain syndrome.
See the full eligibility criteria
Who can join
- Women and men above 18 years old with gender percentages reflective of disease prevalence in the U.S. population
- Individual with diagnosis of overactive bladder with urgency urinary incontinence.
- Individual has at least one urgency urinary incontinence episode on each of three days as determined on a 3-day voiding diary.
- Individual gives written informed consent.
- Individual is mentally competent and able to understand all study requirements.
- Individual is willing and able to complete a 3-day voiding diary and quality of life questionnaire.
- Individual is without pharmacological treatment of overactive bladder (anticholinergic and β3-adrenoceptor agonists) for 2 weeks prior to baseline or longer if the physician judges that the therapeutic effect is still...
- Individual is intolerant of or has an inadequate response to any of anticholinergics, β3-adrenoceptor agonists, onabotulinumtoxinA, or who have undergone percutaneous tibial nerve stimulation (PTNS).
- Individual is determined to be a suitable surgical candidate by physician.
- Individual is appropriate for eCoin treatment based on the US FDA-approved IFU requirements.
What rules you out
- Individual is not appropriate for eCoin therapy based upon the US FDA-approved IFU requirements.
- Individual has clinically significant bladder outlet obstruction. (Suspected bladder outlet obstruction will be initially assessed by uroflow study with those having a maximum flow rate \< 15mL/s requiring additional...
- Individual has predominantly stress urinary incontinence (greater than 1/3 of leaks on baseline diary are stress).
- Individual has an active urinary tract infection at time of enrollment.
- Individual has known polyuria.
- Individual has significant lower urinary tract pain or has been diagnosed with interstitial cystitis or bladder pain syndrome.
- Individual has abnormal post void residual (i.e. greater than 200 cc initially and on repeat testing after double voiding)
- Individual has clinically significant urethral stricture disease or bladder neck contracture. (Suspected disease or contracture will be initially assessed by uroflow study with those having a maximum flow rate \< 15mL/s...
- Individual has chronic venous insufficiency with a history of skin change (hyperpigmentation, lipodermatosclerosis, ulceration) in the ankle region.
- Individual has morbid obesity and in the opinion of the investigator is not a good candidate for the study.
- Individual has had diagnosis of bladder, urethral, or prostate cancer.
- Individual has had a prior anti-stress incontinence sling surgery within the last year.
- Individual is pregnant or intends to become pregnant during the study.
- Individual has the presence of urinary fistula, bladder stone, or interstitial cystitis.
- Individual has uncontrolled diabetes mellitus (Hemoglobin A1C\>7) or diabetes with significant peripheral complications. (Uncontrolled diabetes will be ruled out by blood test excluding those with Hemoglobin A1C\>7).
- Individual has an implantable neurostimulator, pacemaker, or implantable cardiac defibrillator (ICD).
- Individual has been treated with onabotulinumtoxinA in the previous 9 months prior to enrollment, or more time if the principal investigator judges that the therapeutic effect is present.
- Individual has been treated with percutaneous tibial nerve stimulation (PTNS) within the previous 4 weeks prior to enrollment or more time if the principal investigator judges that the therapeutic effect is present.
- Individual is currently using transcutaneous electrical nerve stimulation (TENS) in the pelvic region, back, or legs.
- Individual is aware that he or she will need an MRI scan other than a head/neck/shoulder MRI during the study period.
- Individual has a clotting or bleeding disorder or is using anticoagulant therapies and in the opinion of the investigator is not a good candidate for the study (antiplatelet and anticoagulant therapy may be continued or...
- Individual is neutropenic or immune-compromised.
- Individual has had previous surgery and/or significant scarring at the implant location.
- Individual has ongoing dermatologic condition at the implant site, including but not limited to dermatitis and autoimmune disorders.
- Individual has a clinically significant peripheral neuropathy in the lower extremities.
- Individual has neurogenic bladder dysfunction.
- Individual has pitting edema at implant location (≥ 2+ is excluded).
- Individual has inadequate skin integrity or any evidence of an infection or inflammation in either lower leg.
- Individual has varicose veins and is symptomatic.
- Individual has open wounds, trauma, or prior surgery in the lower extremities.
- Individual has arterial disease in the lower extremities.
- Individual has vasculitis in the lower extremities.
- Individual has bladder stones or neoplasia. (Suspected bladder stones or neoplasia will be ruled out with a urine dipstick showing no more than trace blood, and microscopic analysis (which should be done in that case)...
- In the opinion of the investigator, Individual is not a good candidate for participation in the study.
The study team makes the final eligibility decision.
Where it's taking place
- Homewood, Alabama, United States
- Mobile, Alabama, United States
- Little Rock, Arkansas, United States
- Irvine, California, United States
- Los Angeles, California, United States
- Stanford, California, United States
- Hialeah, Florida, United States
- Atlanta, Georgia, United States
- Chicago, Illinois, United States
- Ankeny, Iowa, United States
- Iowa City, Iowa, United States
- Kansas City, Kansas, United States
- Wichita, Kansas, United States
- Shreveport, Louisiana, United States
- Woodbury, Minnesota, United States
- St Louis, Missouri, United States
- New York, New York, United States
- Portland, Oregon, United States
- West Columbia, South Carolina, United States
- Arlington, Texas, United States
+ 1 more site(s).
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Homewood, Alabama, United States; Mobile, Alabama, United States; Little Rock, Arkansas, United States; Irvine, California, United States; Los Angeles, California, United States; Stanford, California, United States and 15 more location(s). Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.