Detectability of the Bladder With an Early Prototype of the Bladder Sensor

The purpose of this clinical investigation with healthy subjects (defined as subjects without urological problems or lower urinary tract symptoms, assured by pre-defined inclusion and exclusion criteria) is to collect raw measurement data of the urinary bladder region of volunteers with the TENA-PROTO1, in multiple postural positions to evaluate the detectability of the bladder in the intended users and to determine the position criteria for the (future) ultrasound sensor on the lower abdomen. Secondarily, this clinical investigation aims to collect data on the adhesive and supportive belt used to fix the transducer assembly to the lower abdomen by the subject. Furthermore, safety of the subjects will be continously documented such as adverse events (AE) and device deficiencies (DD); AEs, Adverse Device Events (ADE), Severe Adverse Events (SAE), Severe Adverse Device effects (SADE), Unanticipated Serious Adverse Device Effects (USADE) and DDs.

Inclusion criteria

• Men, women and diverse ≥ 35 and <75 years old
• Capability to understand the subject information and to provide conscious informed consent
• Signed informed consent for study participation and data protection regulations
• All subjects with childbearing potential must either be surgically sterile (hysterectomy or tubal ligation) or agree to use a reliable method of contraception with a failure rate of a Pearl-Index less than 1% per year when used consistently and correctly such as implants, injectables, combined oral contraceptives, some intra uterine devices, sexual abstinence or vasectomized partner for at least 4 weeks
• Willingness to conduct a urine pregnancy test for all subjects with childbearing potential
• BMI ≥18.5 kg/m² and <40 kg/m²
• Capability and willingness to follow the following requirements: protocol, current hygiene concept and laboratory safety

Exclusion criteria

• Subjects with urological problems or lower urinary tract symptoms
• Subjects with breached skin, open wounds, sutures or major scar tissue in the suprapubic region.
• Subjects with active implants that can be affected by electromagnetic interference (e.g. pacemaker)
• Subjects with symptoms of constipation or diarrhea
• Subjects who are pregnant or breast feeding
• Known allergies or intolerances to one or several components of the study product
• Alcohol abuse as reported by subject and/ or suspected by investigator that impacts capability to understand the subject information and to provide conscious informed consent in the discretion of the investigator / study personnel
• Drug abuse as reported by subject and/ or suspected by investigator that impacts capability to understand the subject information and to provide conscious informed consent in the discretion of the investigator / study personnel
• Objections of the investigator to the subject's participation in the trial due to medical reasons or any other reason for which the subject should not participate in the opinion of the investigator
• Participation in any clinical investigation with systemic and/or pharmaceutical substances within the last 4 weeks and/or in parallel
• Sponsors, manufacturers or CRO staff