Study on the Patient-Ventilator Asynchrony Analysis Function

NCT ID: NCT06390917

Last Updated: 2024-04-30

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-04-20
• Study Completion Date: 2024-12-24

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.

Conditions

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

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: SINGLE

Study Groups

With PVAs group

With the assistance of PVA function, researchers identify the patient-ventilator asynchronies and take actions to reduce the asynchronies.

Group Type: EXPERIMENTAL

PVA recognition function

Intervention Type: DEVICE

Ventilator with the function of identify and judge PVAs

Without PVAs group

PVA function is not utilized in this arm, researchers identify the patient-ventilator asynchronies by their own and take actions to reduce the asynchronies.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

PVA recognition function

Ventilator with the function of identify and judge PVAs

Intervention Type: DEVICE

Eligibility Criteria

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

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Ming Zhong

OTHER

Sponsor Role: lead

Responsible Party

Ming Zhong

Professor

Responsibility Role: SPONSOR_INVESTIGATOR

Central Contacts

Ming Zhong

Role: CONTACT

zhong.ming@zs-hospital.sh.cn

+86-13817758167

Yaxiaerjiang Muhetaer

Role: CONTACT

yaxxar@163.com

+86-15021891200

Other Identifiers

B2024-082

Identifier Type: -

Identifier Source: org_study_id