Vesair Balloon Confirmatory Trial (VECTOR)

Stopped early · Not applicable

Conditions studied: Stress Urinary Incontinence

In brief

Multicenter, prospective, single-arm study to assess the safety and efficacy of the Vesair Bladder Control treatment in post-menopausal women with Stress Urinary Incontinence (SUI) with follow-up at 1, 3 and 12 months. All subjects will be prospectively treated after the subject has provided informed consent and determination that all study entry criteria have been met.

Key facts

Study ID
NCT03794206
Run by
Solace Therapeutics, Inc.
People needed
20
Starts
2019-02-11
Expected to finish
2022-04-28
Last updated by the study team
2022-06-13

Who can join

Age: any. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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