CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 12 enrolled
Drug / intervention
SpeediCath(R)device
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04250987
NCT04250987N/ACompleted
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Exploratory Investigation of Data Obtained From a Sensor Connected to an Intermittent Catheter

Coloplast A/S·interventional·Posted Jan 31, 2020·Updated Sep 21, 2020

In Brief

A clinical study evaluating SpeediCath(R) for Compliance, Patient. Completed, enrolled 12 participants across 1 site.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCompliance, Patient
CountriesDenmark
Collaborators--

Timeline

N/ACompletedFinished
2020202120222023202420252026
First PostedJan 31, 2020
Enrollment StartMar 23, 2019
Primary CompletionApr 4, 2019
TodayJul 2, 2026
Enrollment to primary: 11 daysPosted 6.4 years ago

Interventions

SpeediCath(R)device

IC SpeediCath ® connected to pressure sensor