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Effect of Mechanical Insufflation–Exsufflation Combined with Closed Suction on Patients with Acute Respiratory Distress Syndrome Receiving Invasive Mechanical Ventilation

Effect of Mechanical Insufflation–Exsufflation Combined with Closed Suction on Patients with Acute Respiratory Distress Syndrome Receiving Invasive Mechanical Ventilation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113842
Enrollment
Unknown
Registered
2025-12-03
Start date
2025-08-21
Completion date
Unknown
Last updated
2026-06-15

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

Conditions

Acute Respiratory Distress Syndrome

Interventions

Ccontrol group:Routine airway secretion management measures for mechanically ventilated patients include elevating the head of the bed by 30°–45°
repositioning the patient every 2 hours with chest percussion and limb mobilization, following the principles of percussing from the outer to the inner areas and from the lower to the upper regions to
performing oral care every 8 hours
using a heat and moisture exchanger to maintain the Y-piece temperature of the ventilator circuit between 34°C and 41°C and relative humidity at 100% to ensure adequate humidification of inspired gase
Intervention group:On the basis of the control group treatment, patients in the intervention group additionally received mechanical insufflation–exsufflation (MI-E) combined with closed suctioning thr
when oxygen saturation decreased and was suspected to be related to airway secretions
when, after excluding ventilator circuit vibration and condensate accumulation, the flow and/or pressure waveform on the ventilator display still showed a saw-tooth pattern
when a reduction in tidal volume during mechanical ventilation was suspected to be associated with increased airway secretions
or when peak inspiratory pressure increased during volume-controlled ventilation, suggesting the presence of upper airway secretions or regurgita

Sponsors

Hebei General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age >= 18 years old; 2. Meet the diagnostic criteria of the new global definition of ARDS in the 2023 edition; 3.The expected duration of mechanical ventilation >= 5 days; 4. Hemodynamic stability: 90 mmHg<= SBP<= 160 mmHg, 50 mmHg<= DBP<= 110 mmHg, and HR < 130 beats/min; 5. The patient or their legal representative consents to participate in this study.

Exclusion criteria

Exclusion criteria: 1. A history of or current presence of bullous emphysema, un drained pneumothorax or populations at high risk of pneumothorax, mediastinal emphysema, recent barotrauma, and tracheoesophageal fistula 2. Active intrapulmonary hemorrhage or hemoptysis; 3. Increased intracranial pressure; 4. Ruptured tympanic membrane.

Design outcomes

Primary

MeasureTime frame
Sputum volume;

Secondary

MeasureTime frame
Arterial blood gas parameters;Vital signs;Duration of mechanical ventilation;Length of ICU stay;28-day mortality;Clinical Pulmonary Infection Score;The white blood cell;Procalcitonin;C-reactive protein;

Countries

China

Contacts

Public ContactLiu Chunxia

Hebei General Hospital

lcx666@126.com+86 155 1185 0797

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 21, 2026