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NCT05232253 · ClinicalTrials.gov registry record · NA

Cystoealstometer (Bladder Monitor Device)-Home Use

A NA study of Urinary Bladder, Neurogenic, sponsored by University of Iowa.

Active
Registry status
NA
Development phase
30
Enrollment target
1
Study location

NCT05232253: Active NA study of Urinary Bladder, Neurogenic, sponsored by University of Iowa.

NCT05232253 is a NA study of Urinary Bladder, Neurogenic that is active but no longer recruiting, run by University of Iowa. The registered enrollment target is 30 participants, below the 67-participant average among 7 other Urinary Bladder, Neurogenic trials with a reported enrollment target (55% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05232253, a NA study of Urinary Bladder, Neurogenic, is active but no longer recruiting, sponsored by University of Iowa.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
30 participants
Enrollment target
1
Study location

Study Summary

The investigators have developed a novel pressure monitoring device called a 'cystoelastometer' that connects to a drainage end ofastandard urinary catheters that are used by patients with a neurogenic bladder on daily clean intermittent catheterization. The device has already been demonstrated to be accurate in measuring bladder pressure compared to the gold standard urodynamics that are performed in the clinic or hospital. This study will assess the patients and care givers ability and experience using the cystoelastometer device in a home setting.

Primary Outcome

Utilization study of novel external cystoelastometer device - Home bladder pressure and volume monitor recorded in terms of cm H2O pressure and urine evacuation device with volume measurement in terms of milliliters.

Interventions

  • DEVICE Cystoelastometer - Urodynamics Testing

Study Locations (1)

Iowa

  • University of Iowa Hospital and Clinics - Iowa City

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2021-01-18
Est. Completion 2027-02-01
Phase NA
University of Iowa

228 total trials

What the registry record for NCT05232253 still lists

NCT05232253 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 67-participant average among 7 other Urinary Bladder, Neurogenic trials with a reported enrollment target (55% lower).

The record links to 1 condition, with Urinary Bladder, Neurogenic appearing as the primary indexed condition, and to 1 intervention - of which Cystoelastometer - Urodynamics Testing is the first listed.

NCT05232253 reports a single indexed study location in Iowa.

Frequently Asked Questions

What is clinical trial NCT05232253 about?

NCT05232253 is a clinical study titled "Cystoealstometer (Bladder Monitor Device)-Home Use". The investigators have developed a novel pressure monitoring device called a 'cystoelastometer' that connects to a drainage end ofastandard urinary catheters that are used by patients with a neurogenic bladder on daily clean intermittent catheterization. The device has already been demonstrated to b...

What is the current status of trial NCT05232253?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 30 participants. The study started on 2021-01-18. Estimated completion is 2027-02-01.

What conditions does trial NCT05232253 study?

This clinical trial studies the following conditions: Urinary Bladder, Neurogenic.

What interventions are being tested in trial NCT05232253?

The interventions under investigation include: Cystoelastometer - Urodynamics Testing (DEVICE).

Who is sponsoring clinical trial NCT05232253?

This trial is sponsored by University of Iowa, which has 228 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05232253 being conducted?

This trial has 1 study location across Iowa. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT05232253, the US trial registry maintained by the National Library of Medicine. NCT05232253 (small enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.