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NCT01885793 · ClinicalTrials.gov registry record

Cuff Pressure in Patients: Manometer vs Invasive Pressure Monitoring Setup

A clinical trial of Anesthesia Intubation Complication, sponsored by Senthil G. Krishna.

Completed
Registry status
220
Enrollment target
1
Study location

NCT01885793: Completed study of Anesthesia Intubation Complication, sponsored by Senthil G. Krishna.

NCT01885793 is a study of Anesthesia Intubation Complication that has completed, run by Senthil G. Krishna. The registered enrollment target is 220 participants. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01885793, a study of Anesthesia Intubation Complication, has completed, sponsored by Senthil G. Krishna.

COMPLETED
Registry status
220 participants
Enrollment target
1
Study location

Study Summary

This is a prospective study looking at ways to measure the cuff pressure of cuffed endotracheal tubes (ETTs). We will be comparing a hand-held manometer (MM) to the transducer of an invasive pressure monitoring setup (IPMS), which is commonly used for arterial or central venous pressure monitoring. The investigators previously did this study in vivo with ETTs in polyvinyl chloride (PVC) "tracheas" and we found that there is good correlation between the pressure readings using the MM and the IPMS. The purpose of the current study is to validate the in vitro findings in clinical situations.

Primary Outcome

Intracuff pressure is measured via handheld manometer and by using the transducer of an invasive pressure monitoring device.

Interventions

  • DEVICE Cuffed endotracheal tube

Study Locations (1)

Ohio

  • Nationwide Children's Hospital - Columbus

Trial Details

FieldValue
Enrollment Target 220 participants
Start Date 2013-04
Est. Completion 2013-12
Senthil G. Krishna

5 total trials

What the finished NCT01885793 record still lists

NCT01885793 is an observational study that tracks outcomes without assigning an intervention. The registered 220 participants enrollment target is mid-sized for trials with a published cap.

The record links to 1 condition, with Anesthesia Intubation Complication appearing as the primary indexed condition, and to 1 intervention - of which Cuffed endotracheal tube is the first listed.

NCT01885793 reports a single indexed study location in Ohio.

Frequently Asked Questions

What is clinical trial NCT01885793 about?

NCT01885793 is a clinical study titled "Cuff Pressure in Patients: Manometer vs Invasive Pressure Monitoring Setup". This is a prospective study looking at ways to measure the cuff pressure of cuffed endotracheal tubes (ETTs). We will be comparing a hand-held manometer (MM) to the transducer of an invasive pressure monitoring setup (IPMS), which is commonly used for arterial or central venous pressure monitoring. ...

What is the current status of trial NCT01885793?

This trial is currently completed. The enrollment target is 220 participants. The study started on 2013-04. Estimated completion is 2013-12.

What conditions does trial NCT01885793 study?

This clinical trial studies the following conditions: Anesthesia Intubation Complication.

What interventions are being tested in trial NCT01885793?

The interventions under investigation include: Cuffed endotracheal tube (DEVICE).

Who is sponsoring clinical trial NCT01885793?

This trial is sponsored by Senthil G. Krishna, which has 5 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01885793 being conducted?

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

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Source: ClinicalTrials.gov NCT01885793, the US trial registry maintained by the National Library of Medicine. NCT01885793 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.