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Exploratory Investigation of Data Obtained From a Sensor Connected to an Intermittent Catheter

NCT04250987 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2020-09-21

Study results available
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Summary

The purpose of the investigational device in the proposed clinical investigation is to capture pressure data prior to and during voiding using a CE-marked commercially available catheter.

Conditions

  • Compliance, Patient

Interventions

DEVICE

SpeediCath(R)

IC SpeediCath ® connected to pressure sensor

Sponsors & Collaborators

  • Coloplast A/S

    lead INDUSTRY

Principal Investigators

  • Fredrik Ceder, M.Sc · Head of Clinical Operations

Study Design

Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-03-23
Primary Completion
2019-04-04
Completion
2019-04-04

Countries

  • Denmark

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 NCT04250987 on ClinicalTrials.gov