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Completed

NCT Number: NCT04030208

Evaluating Safety and Efficacy of Umbulizer in Patients Requiring Intermittent Positive Pressure Ventilation

Randomized, control crossover study comparing Umbulizer's efficacy to traditional mechanical ventilators

Completed

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Key information

Age range

18 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Services Hospital

Lahore, Punjab Province, Pakistan

About this study

Mechanical ventilators cost tens of thousands of dollars, rendering them difficult for low and middle income countries to procure. Given chronic shortages of these devices in places like Pakistan, patients are often ventilated manually with Ambu Bags for hours or days. This method is not suitable for long term ventilation and is extremely life threatening.

Umbulizer seeks to reduce preventable deaths due to ventilator scarcity by providing a reliable alternative. The device is accurate, low-cost, and portable, and is an ideal solution for treating patients with respiratory diseases in low-resource settings. The primary objective of this study is to test efficacy and determine non-inferiority of this device in comparison to ventilation provided by traditional ventilators. Secondary objectives of this study include:

  • Testing safety of the device for use over a predetermined period of time
  • Evaluating patient comfort during ventilation with this device
  • Assessing ease of use of this device for doctors and medical staff

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients needing mechanical ventilation

Exclusion criteria

  • Patients with significant airway resistance (i.e. severe chronic obstructive pulmonary disease or asthma) where clinical investigator is concerned about gas trapping or barotrauma
  • Patients with very low lung compliance (i.e. severe acute respiratory distress syndrome or restrictive disease) where clinical investigator is concerned about problems delivering sufficient tidal volume or end expiratory pressure
  • Patients who experienced a myocardial infarction within the last 6 weeks
  • Patients who are determined by a clinical investigator to be too hemodynamically unstable to be enrolled

Treatment and study plan

Umbulizer

Device

Umbulizer is a reliable, user-friendly, and portable system that provides consistent air to the patient by quantitatively delivering a pre-determined tidal volume, inhale/exhale (I/E) ratio, peak pressure, and breathing rate (BPM). It can be configured to deliver either controlled ventilation or assist-controlled ventilation.

Traditional Mechanical Ventilator

Device

A medical device designed to artificially perform breathing functions for patients who are unable to adequately perform these functions on their own.

Primary outcomes

  1. Partial Pressure of Carbon Dioxide (PaCO2)

    Time frame: 2 hours

    PaCO2 in mmHg at t = 1 hr (from Arterial Blood Gas or ABG readings) when patient is on Umbulizer compared to PaCO2 at t = 1 hr when patient is on a traditional mechanical ventilator

  2. pH

    Time frame: 2 hours

    pH at t = 1 hr (from ABG readings) when patient is on Umbulizer compared to pH at t = 1 hr when patient is on a traditional mechanical ventilator

Secondary outcomes

  1. Number of Adverse Events

    Time frame: 2 hours

    Number of adverse events on Umbulizer compared to on a traditional ventilator

Other outcomes

  1. Level of Comfort

    Time frame: 2 hours

    Level of comfort on Umbulizer will be determined based on a 4-point scale assessing a combination of indicators (1 point will be assigned for the absence of each of the following: substantial deviation of heart rate from baseline, substantial deviation of blood pressure from baseline, grimacing, diaphoresis).

  2. Ease of Use

    Time frame: 2 hours

    Umbulizer's ease of use will be determined based on survey responses by doctors/medical staff at the end of each experiment

  3. Partial Pressure of Oxygen (PaO2)

    Time frame: 2 hours

    PaO2 in mmHg at t = 1 hr (from ABG readings) when patient is on Umbulizer compared to PaO2 at t = 1 hr when patient is on a traditional mechanical ventilator

  4. O2 Saturation

    Time frame: 2 hours

    O2 saturation (from pulse oximeter) when patient is on Umbulizer compared to when patient is on a traditional mechanical ventilator

Sponsors and collaborators

Lead sponsor

Umbulizer LLC

Industry

Registry information

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Jul 23, 2019
Registry last updated
Aug 6, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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