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A Protocol to Wean From Noninvasive Mechanical Ventilation

A Protocol to Wean From Noninvasive Mechanical Ventilation

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01535755
Enrollment
80
Registered
2012-02-20
Start date
2010-07-31
Completion date
2011-05-31
Last updated
2013-07-16

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

Conditions

Ventilator Weaning

Keywords

noninvasive mechanical ventilation, ventilator weaning

Brief summary

The investigators use a protocol to wean from noninvasive mechanical ventilation.

Detailed description

Design: Prospective, randomized, controlled trial, with 2 groups: study (protocol weaning group) and control (clinicians' order weaning group). Setting: Respiratory Intensive Care Unit (RICU). Subjects: Patients \>18 yr, noninvasive mechanical ventilation \>24 hours. Interventions and measurements: Study group (weaning as the protocol) and control group (weaning as the clinicians' order); recording of clinical variables at admission and during RICU stay, and end-point variables (noninvasive mechanical ventilation day, RICU and hospital stay, RICU mortality. Expected results: the protocol group's noninvasive mechanical ventilation days is less than clinicians' order group.

Interventions

DEVICEprotocol

In this group, the patients were weaned as the protocol.

OTHERphysician's orders

In this group, the patients were weaned as the clinicians' order.

Sponsors

Duan jun
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
NONE

Eligibility

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

Inclusion criteria

1. noninvasive mechanical ventilation \> 24 hours. 2. age \>18 years

Exclusion criteria

1. severe cerebraI,heart,hepatic and renal faiIure. 2. facial or cranial trauma or surgery. 3. facial abnormalities. 4. recent gastric or esophageal surgery. 5. active upper gastrointestinal bleeding. 6. large amount of sputum with weak cough ability 7. lack of co-operation.

Design outcomes

Primary

MeasureTime frameDescription
The duration of noninvasive mechanical ventilationfrom admission to ICU to discharge from it (average of 4 weeks)The duration of noninvasive mechanical ventilation was measured from the patients admitted to ICU to discharged from it,an expected average of 4 weeks.

Secondary

MeasureTime frameDescription
The successful weaning ratefrom admission to ICU to discharge from it (average of 4 weeks)The successful weaning rate was measured from the patients admitted to ICU to discharged from it, an expected average of 4 weeks.
The length of ICU daysfrom admission to ICU to discharge from it (average of 4 weeks)The length of ICU days was measured from the patients admitted to ICU to discharged from it, an expected average of 4 weeks.
The intubation rate during the studyfrom admission to ICU to discharge from it (average of 4 weeks)The intubation rate during the study was measured from the patients admitted to ICU to discharged from it, an expected average of 4 weeks.
The mortality during the studyfrom admission to ICU to discharge from it (average of 4 weeks)The mortality during the study was measured from the patients admitted to ICU to discharged from it, an expected average of 4 weeks.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026