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Study of Angles of Postural Drainage in Neurocritical Patients with Pneumonia

Study of Angles of Postural Drainage in Neurocritical Patients with Pneumonia

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100042155
Enrollment
Unknown
Registered
2021-01-14
Start date
2021-01-31
Completion date
Unknown
Last updated
2021-04-12

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

Conditions

Severe neurological disease with pneumonia

Interventions

experimental group:Bedside elevation 30 degrees posture drainage
control group:Bedside elevation 0 degrees posture drainage

Sponsors

Guangdong Sanjiu Brain Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Severe neurological patients with pneumonia (all patients with artificial airway), aged 18-65 years, regardless of gender; 2. It meets the diagnostic criteria of pneumonia (X-ray infiltration shadow of imaging or CT lung exudation and clinical laboratory test results); Clinical pulmonary infection score (CPIS score) >= 5 points; 3. Patients with stable hemodynamics and stable vital signs; 4. Patients or legal representatives agreed to participate in the trial and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. The difference of blood pressure and systolic pressure of both upper limbs is > 10 mmHg , the upper limb is fractured or there is an implant in the upper arm of one limb; 2. Those with severe liver and kidney dysfunction or severe basic lung diseases, such as chronic obstructive pulmonary disease and lung cancer; 3. Persons with special requirements and contraindications of body position, such as thoracic or spinal fractures, recent massive hemoptysis and history of traumatic fractures, inability to tolerate the required body position, risk of massive bleeding due to anticoagulant therapy, severe craniocerebral injury with cranial hypertension such as fracture, brain stem injury and spinal cord injury; 4. It is not suitable for this researcher to assess the risk of aspiration, and there are patients with esophagectomy, stomach resection or lung resection within half a year; 5. The attending doctor thinks that it is not suitable to participate in this trial.

Design outcomes

Primary

MeasureTime frame
Clinical pulmonary infection score;

Secondary

MeasureTime frame
Blood gas results;intracranial pressure;Mechanical ventilation index;Infection indicators (white blood cell count, PCT, C-reactive protein);Risk score of aspiration;

Countries

China

Contacts

Public ContactZhao Anna

Guangdong Sanjiu Brain Hospital

109545437@qq.com+86 15814832989

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026