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Rate of Postpyloric Migration of Spiral Nasojejunal Tubes in Brain Injured Patients

Rate of Postpyloric Migration of Spiral Nasojejunal Tubes in Brain Injured Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00562146
Enrollment
120
Registered
2007-11-21
Start date
2007-12-31
Completion date
2008-09-30
Last updated
2008-10-28

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

Conditions

Acute Brain Injury

Keywords

nutrition, enteral access

Brief summary

The success rate of unguided nasojejunal feeding tube insertion will be determined in acute brain injured patients. Factors influencing tube self-progression will be evaluated.

Detailed description

Nutrition support is important in brain injured patients. Several studies have shown that small bowel feeding compared with gastric feeding may be associated with a reduction in pneumonia in critically ill patients. The Canadian Clinical Practice Guidelines recommended that small bowel feedings should be considered for patients at high risk for intolerance to enteral nutrition. There are several methods to place postpyloric tube, but there is a high success rate with endoscopic or radiological assistance. However, they are time consuming procedures, which is of limited availability at bedside and requires trained staff. Nasojejunal tube with spiral end (Flocare Bengmark NJ tube) has been used for bedside placement for 10 years. But only limited data are available for success rate, especially in brain injured patients. The aim of this study is to access the success rate and influencing factors of spiral end nasojejunal tube in such a population.

Interventions

PROCEDUREplacement of spiral nasojejunal tube

spiral nasojejunal tube will be placed after enrollment of the patients

Sponsors

Capital Medical University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Acute brain injured patients admitted to Neuro-ICU

Exclusion criteria

* Patients' stay in ICU shorter than 3 days * Patients with contraindication to naso-feeding tube placement

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026