Application of siphon drainage in blind nasoenteric catheterization in patients with severe neurosurgery

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2400082317

Enrollment

Unknown

Registered

2024-03-26

Start date

2024-03-26

Completion date

Unknown

Last updated

2024-04-01

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

Conditions

Neurosurgical severe disease

Interventions

Experimental group:The blind nasoenteric tube was inserted by siphon drainage

Control group:Blind nasoenteric tube insertion was performed by conventional method

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Critically ill patients with consciousness disorder, GCS score =8 points; (2) Patients with scores =2 in the Aspiration Risk Assessment Form; (3) No obvious intestinal absorption and digestive dysfunction; (4) The patient's family members sign the informed consent.

Exclusion criteria

Exclusion criteria: (1) Combined with enteral nutrition contraindications; (2) serious insufficiency of heart and kidney function; (3) Combined nasal trauma surgery history; (4) History of epistaxis, space occupying in nasal cavity and edema of throat; Distal intestinal obstruction or perforation.

Design outcomes

Primary

Measure	Time frame
One-time tube placement success rate;	—

Countries

China

Contacts

Public ContactWU Yuyan

Tangdu Hospital, Fourth Milital ry Medical University

1322204303@qq.com+86 135 7253 9961

Outcome results

None listed

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