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Study on the Patient-Ventilator Asynchrony Analysis Function

Study on the Patient-Ventilator Asynchrony Analysis Function

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06390917
Enrollment
30
Registered
2024-04-30
Start date
2024-04-15
Completion date
2025-04-30
Last updated
2026-09-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

To Study the Incidence of Patient-ventilator Asynchronization in Two Groups of Patients Under Two Conditions With PVA Unsynchronization Analysis Function

Brief summary

In this study, the incidence of patient-ventilator asynchronism in two groups of patients was studied when the ventilator was prompted by the PVA asynchronism analysis function

Detailed description

Incidence of patient-computer dyssynchrony events: defined as the proportion of patient-computer dyssynchrony events in the total number of cycles during the patient trial. The observation period began 48 hours after the participants met the inclusion and exclusion criteria and signed the informed consent, and the data collection was stopped 48 hours later.

Interventions

DEVICEPVA recognition function

Ventilator with the function of identify and judge PVAs

Sponsors

Ming Zhong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Adults (≥18 years) requiring invasive mechanical ventilation 2. Patiens had spontaneous breathing; 3. Agreed to participate in the trial and signed an informed consent

Exclusion criteria

1. Patients with contraindications to esophageal catheter insertion and inability to monitor esophageal pressure; 2. pregnant women; 3. patients with severe central nervous system damage or neuromuscular related diseases; 4. Participating in other clinical research projects; 5. Patients deemed unsuitable by the investigator

Design outcomes

Primary

MeasureTime frameDescription
Incidence rate of PVAs48 hoursPercentage of the number of respiratory cycles in which human-machine asynchronous events occurred in the total number of respiratory cycles in each patient during the trial

Secondary

MeasureTime frameDescription
The proportion of PVAs that were identified by the investigator among the total PVAs during the trial48 hours
Incidence of PVA within half an hour before and after the interventionHalf an hour before and after the intervention
Accuracy of PVA recognition function48 hoursCompare manual audit and machine judgment

Countries

China

Contacts

PRINCIPAL_INVESTIGATORMing Zhong

Shanghai Zhongshan Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 16, 2026