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NCT00562146 Clinical Trial

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

Acute Brain Injury Clinical Trial

Official title:
Rate of Postpyloric Migration of Spiral Nasojejunal Tubes in Brain Injured Patients

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00562146
Other study ID # BJTTH-ICU-07-011
Secondary ID BJTTH-ICU-07-011
Status Completed
Phase N/A
First received November 20, 2007
Last updated October 27, 2008
Start date December 2007
Est. completion date September 2008

Study information
Verified date October 2008
Source Capital Medical University
Contact n/a
Is FDA regulated No
Health authority China: Ministry of Health
Study type Observational

Clinical Trial 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.

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.

Recruitment information / eligibility
Status Completed
Enrollment 120
Est. completion date September 2008
Est. primary completion date September 2008
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

Intervention

Procedure:
• placement of spiral nasojejunal tube
spiral nasojejunal tube will be placed after enrollment of the patients

Locations
Country Name City State
China ICU, Beijing Tiantan Hospital, Capital Medical University Beijing Beijing

Sponsors (1)
Lead Sponsor Collaborator
Capital Medical University

Country where clinical trial is conducted

China, 

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