Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

UK PureWick™ At-Home Pilot Study

The UK PureWick™ At-Home Study is being carried out to see how well the PureWick™ Collection System works for women who use it at home instead of a traditional catheter. Traditional catheters are placed inside the body. The PureWick™ Collection System is different, it's placed outside the body . In this study, researchers want to find out: how effective the PureWick™ Collection System is in helping women manage urine collection at home, whether patients prefer using PureWick™ Collection System over the usual catheter, how it affects their sleep, and overall well-being.The PureWick™ Collection System is intended for the treatment of patients who leak urine (called urine incontinence). The PureWick™ Collection System is designed to help manage urine in female patients without needing to insert a urinary catheter into the body.

Participants needed: 95
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Becton, Dickinson and CompanyUpdated: Jul 13, 2026Locations: 4
Eligibility criteria

Adult Female Subjects >18 years of age at the time of signing the informed conse... [+4]

Has frequent episodes of bowel incontinence without a fecal management system in... [+9]

Status: Recruiting

The Continuity Study

A before and after interventional cohort study comparing intermittent blood pressure measurement using the oscillometric arm cuff to continuous noninvasive blood pressure (cNIBP) measurement using the VitaWave finger cuffs in subjects undergoing elective surgery in an outpatient setting.

Participants needed: 188
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Becton, Dickinson and CompanyUpdated: Jul 8, 2026Locations: 1
Eligibility criteria

Signed informed consent [+3]

Patient who is known to be pregnant [+6]

Status: Recruiting

Personal BP - CAI Study

A single-center, prospective, observational pilot of the Cerebral Adaptive Index for assessing personalized blood pressure targets

Participants needed: 120
Trial details
Age: 45+Biological sex: AllType: InterventionalSponsor: Becton, Dickinson and CompanyUpdated: Jul 8, 2026Locations: 1
Eligibility criteria

Signed informed consent [+5]

Non-English speaking [+3]