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Monitoring for Low Minute Ventilation Post SurgeryNCT03039881

Evaluation of Non-Invasive Respiratory Volume Monitor

An observational study of Monitoring for Low Minute Ventilation Post Surgery, run by Tufts Medical Center at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This observational study investigates the validity and utility of a new, non-significant risk, FDA approved respiratory monitor, ExSpiron, in the perioperative course of patients undergoing elective surgery under general anesthesia. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Non-Invasive Respiratory Volume Monitor
Type of treatment
Medical device
How many people
150 participants
Where
1 siteUnited States
Study dates
9 Jan 2015to 8 Jan 2019
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Adult patients undergoing elective surgery with general anesthesia

Who may be able to join

  • Adult patients undergoing surgery with general anesthesia and positive pressure ventilation, patient's ≥80 pounds and who are able to give informed consent.

Who cannot join

  • Patients unable to give informed consent. Any patient whose condition or procedure will not allow for placement of the electrode PadSet

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Tufts Medical Center

    Boston, Massachusetts, 02111

Other trials in United States

About this study

Official title: Blinded Observational Study to Evaluate a Non-Invasive Respiratory Volume Monitor in the Post-Anesthesia Care Unit and on the General Hospital Floor

This observational study investigates the validity and utility of a new, non-significant risk, FDA approved respiratory monitor, ExSpiron, in the perioperative course of patients undergoing elective surgery under general anesthesia. The study patients will be monitored before, during and after surgery, in post-anaesthesia care unit (PACU) and recovery room for the first post-operative night. The physiologic data will not be used or influence the standard of care for subjects. It is anticipated that this monitor may be able to improve perioperative care in the future.

Read the detailed description

Aim and Hypotheses Currently, there is no objective measure of early respiratory indicators for developing respiratory compromise in surgical patients. Current respiratory assessment in non-intubated patients relies on oximetry data and subjective clinical assessment. Pulse oximetry has been extremely helpful in recognizing oxygen desaturations but it is a late indicator of respiratory decline. New advances in technology and digital signal processing have led to the development of an impedance based Respiratory Volume Monitor (RVM). The RVM (ExSpiron™, Respiratory Motion, Inc.; Waltham, MA) has been shown to provide accurate real-time, continuous, non-invasive measurements of tidal volume (TV), minute ventilation (MV) and respiratory rate (RR) in general patient population.

Hypotheses

Primary:

Low minute ventilation (LMV) defined as sustained LMV<40% minute ventilation predicted (MVPRED) based on IBW following opioid administration correlates with adverse clinical outcomes in PACU or on the floor including:

  • O2 desaturation, atelectasis, respiratory status requiring advanced monitoring
  • respiratory interventions such as O2 administration, continuous positive airway pressure CPAP, BiPAP,
  • incidence of ICU transfer and/or increase in PACU and/or general hospital floor (GHF) length of stay (LOS).

Secondary:

  • 1. Decreased MV defined as sustained MV<80% MVPRED based on IBW before opioid administration correlates with adverse clinical outcomes as defined above.
  • 2. Patients with decreased MV prior to opioid administration will be more likely to develop LMV after standard opioid administration compared to patients with normal MV defined as MV ≥ 81% MVPRED based on ideal body weight (IBW)

Rationale Continuous respiratory monitoring using the ExSpiron System will be particularly beneficial to patients in the post-anesthesia environment. Assessment and management of respiratory function and early intervention when indicated is a multifaceted, complex task often complicated by the lack of a cohesive and continuous monitoring system to guide clinical decisions. The ExSpiron system is designed for these patients and is intended to address some of the limitations of the current generation of hospital monitors and to provide healthcare providers with continuous real-time data regarding the patient's respiratory status. Recent data has shown that stratification of patients based on the RVM's MV as % of predicted MV (MVPRED), prior to opioid dosing has made it possible to identify patients who are at risk for further decreases in MV and opioid-induced respiratory depression (OIRD).

  1. In the spontaneously breathing, non-ventilated patient, current monitoring devices do not provide continuous, objective non-invasive, continuous real time information of the important respiratory parameters TV, MV \& RR.
  2. Current monitoring of non-intubated patients mostly relies on subjective clinical assessment, oximetry data, and rarely end-tidal carbon dioxide CO2 measurements. In appropriate clinical settings, the ExSpiron system can provide direct quantitative measure of ventilation parameters for use in clinical assessment and trend prediction as well as response to medications and other interventions to allow for more efficient clinical decision making.
  3. Current technologies do not provide for a continuity of care between the PACU and the general hospital floor.
Being tested
Non-Invasive Respiratory Volume Monitor
Keywords
Minute ventilation, ExSpiron monitor

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Non-Invasive Respiratory Volume MonitorDevice

    The device requires the application of a monitoring PadSets to the patient's skin similar to EKG electrodes and, as such, poses minimal risk.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Low minute ventilation

    Low minute ventilation (LMV) defined as sustained LMV<40% minute ventilation predicted (MVPRED) based on IBW following opioid administration correlates with adverse clinical outcomes in PACU and on the floor

    Measured: Post-operatively in PACU and general patient' floor up to 24 hours after completion of surgery

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted1 Feb 2017 (estimated)
  2. Study start9 Jan 2015
  3. Primary completion8 Jan 2019
  4. Study completion8 Jan 2019

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
150 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03039881
Sponsor's protocol ID
11544
Status last verified
Jan 2019
First submitted
27 Jan 2017
Last updated
9 Jan 2019
Results posted
No
FDA-regulated device
Yes
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Monitoring for Low Minute Ventilation Post Surgery, run by Tufts Medical Center at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 9 Jan 2019. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Low minute ventilation (time frame: Post-operatively in PACU and general patient' floor up to 24 hours after completion of surgery). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Jan 2019.

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