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Study on the clinical application effect of portable visual nasoenteric tube placement in severe patients

Study on the clinical application effect of portable visual nasoenteric tube placement in severe patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400089330
Enrollment
Unknown
Registered
2024-09-05
Start date
2024-09-16
Completion date
Unknown
Last updated
2024-09-09

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

Conditions

Disease of digestive tract

Interventions

Experimental group:A portable visual nasoenteric tube was placed near the bed
Control group:Nasoenteric tube was placed under the guidance of conventional ultrasound

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Has the indication of naso-intestinal tube placement; (2) Over the age of 18; (3) Family members give informed consent and sign the consent form.

Exclusion criteria

Exclusion criteria: ? Hemodynamic instability; ? Severe coagulation dysfunction; ? Active bleeding of digestive tract; ? severe nasopharyngeal stenosis or oesophago-related disease; ? gastric fundus esophageal varices; ? Pyloric obstruction, gastrointestinal diversion and other diseases.

Design outcomes

Primary

MeasureTime frame
One-time tube placement success rate;Piping adjustment;Catheter replacement;Catheterring time;Catheter tip position;Catheter-related complications;—

Secondary

MeasureTime frame
Changes of vital signs during catheterization;Costs associated with tube placement;Patient's recovery;—

Countries

China

Contacts

Public ContactYu Xu

West China Hospital, Sichuan University

121043156@qq.com+86 189 8060 6978

Outcome results

None listed

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