Construction and clinical evaluation of the standard procedure for the prevention of aspiration in critically ill neurosurgical patients

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2200055812

Enrollment

Unknown

Registered

2022-01-20

Start date

2022-01-31

Completion date

Unknown

Last updated

2023-06-26

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

Conditions

neurosurgery

Interventions

control group:none

experimental group:Application intervention process

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged 18 years and over; 2. Enteral nutrition for 24 h after nasogastric feeding; 3. The patient (or the family member of the unconscious patient) gave informed consent to participate in the study.

Exclusion criteria

Exclusion criteria: 1. Those who died or were transferred out of the study within 1 day of inclusion; 2. The patient's participation in the study was not approved by the competent physician or family members.

Design outcomes

Primary

Measure	Time frame
Incidence of aspiration;	—

Secondary

Measure	Time frame
Proportion of aspiration pneumonia;	—

Countries

China

Contacts

Public ContactXiao Qian

Capital Medical University

Julia.xiao@163.com+86 15210756682

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026