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Clinical trialNCT03794206TerminatedInterventional

Vesair Balloon Confirmatory Trial (VECTOR)

SponsorSolace Therapeutics, Inc.Enrollment20Stress Urinary Incontinence
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

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.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

8 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Womancare

    Arlington Heights, Illinois, United States

  • Regional Urology

    Shreveport, Louisiana, United States

  • Chesapeake Urology

    Hanover, Maryland, United States

  • Chesapeake Urology

    Owings Mills, Maryland, United States

  • Premier Medical Group of the Hudson Valley

    Poughkeepsie, New York, United States

  • Women and Infants Dept of Urogynecology

    Providence, Rhode Island, United States

  • Urology of Virginia

    Virginia Beach, Virginia, United States

  • Washington Urology

    Kirkland, Washington, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
11 Feb 2019
Primary completion
26 Aug 2019
Completion
28 Apr 2022
Last update posted
13 Jun 2022
Registered enrollment
20
Registry id
NCT03794206

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.