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Feasibility of the UriCap-F for Urine Collection in Hospitalized Women

NCT02530372 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2015-09-18

No results posted yet for this study

Summary

The study will evaluate safety and effectiveness of the UriCap-F, a non-invasive urine collection device for women, in hospitalized patients who would otherwise be treated with an indwelling catheter, pads or diapers.

Conditions

Interventions

DEVICE

UriCap-F

non-invasive urine collection device for women

Sponsors & Collaborators

  • G.R. Dome Medical Ltd.

    lead INDUSTRY

Principal Investigators

  • Elad Schiff, MD · No affiliation

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-09-30
Primary Completion
2015-11-30
Completion
2015-11-30

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Entities

Diseases

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 NCT02530372 on ClinicalTrials.gov