Phase
Condition
Enuresis
Urinary Incontinence
Overactive Bladder
Treatment
BTL EMSELLA Sham Treatment
BTL EMSELLA Active treatment
Clinical Study ID
Ages 18-100 Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Subject provides written informed consent and HIPAA authorization before any studyprocedures are conducted
Age greater than 18
Subject has a body mass index (BMI) < 37 kg/m2
Subject has stress urinary incontinence, urge incontinence, or mixed urinaryincontinence as determined by the QUID;
Subject is willing to continue level of core exercise currently being performed ornot performed during the study (e.g. gym, Pilates, yoga);
Subject is willing to maintain her current prescription and over the countermedications throughout the study without changing them;
Subject agrees to comply with the study procedures and visits.
Exclusion
Exclusion Criteria:
Subject has used the BTL EMSELLA device previously;
Subject has any significant pelvic organ prolapse; stage III or greater
Subject is unwilling to maintain current level of exercise throughout the study;
Subject planning to have surgery during the study;
Subject has untreated malignancy;
Subject is pregnant, planning to get pregnant or within 3 months postpartum;
Subject has a pacemaker;
Subject has and implant or IUD containing metal;
Subject has piercing between the waist and knees and is not willing to remove itbefore each treatment;
Subject is using a pessary or other anti-incontinence device
Subject has implanted defibrillator, implanted neurostimulator
Subject has metal implants
Subject has a drug pump
Study Design
Study Description
Connect with a study center
Boston Urogynecology Associates
Cambridge, Massachusetts 02138
United StatesActive - Recruiting
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