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A Feasibility Study With a Novel, Dynamic and Disposable Over-the-counter Device for Stress Urinary Incontinence

NCT04325477 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 26

Last updated 2020-04-07

No results posted yet for this study

Summary

This study was designed as an open label, feasibility, single-center, cross-over prospective study in women with stress urinary incontinence. Subjects served as their own control.

Conditions

  • Stress Urinary Incontinence

Interventions

DEVICE

Nolix Device

The Nolix device is a single use, dynamic, and soft flexible intra-vaginal device for temporary management of SUI

Sponsors & Collaborators

  • Gynamics LTD

    lead INDUSTRY

Principal Investigators

  • Boris Friedman, Dr · Carmel Medical Center

Study Design

Purpose
TREATMENT
Masking
NONE
Model
SEQUENTIAL

Eligibility

Min Age
21 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-10-31
Primary Completion
2018-10-30
Completion
2018-10-30

Countries

  • Israel

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04325477 on ClinicalTrials.gov