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Limited Long Term Survival in Patients After In-hospital Intestinal Failure Requiring Total Parenteral Nutrition

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02189993
Recruitment Status : Completed
First Posted : July 15, 2014
Last Update Posted : July 17, 2014
Sponsor:
Information provided by (Responsible Party):
Leendert Oterdoom, VU University Medical Center

Study Description
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Brief Summary:

The purpose of this study is to determine what the long term survival is after in hospital use of total parenteral nutrition due to intestinal failure.

Earlier studies only followed patients for a maximum of 6 months or included only very specific patients. We were interested in all patients in our hospital and followed them for up to 2 years.


Condition or disease
Nutrition Disorders

Detailed Description:
Extensive description is not desired
Study Design
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Study Type : Observational
Actual Enrollment : 437 participants
Observational Model: Cohort
Time Perspective: Retrospective
Official Title: Limited Long Term Survival in Patients After In-hospital Intestinal Failure Requiring Total Parenteral Nutrition
Study Start Date : January 2010
Actual Primary Completion Date : April 2012
Actual Study Completion Date : October 2013

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Groups and Cohorts
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Group/Cohort
Total Parenteral Nutrition Use
The cohort investigated consisted of patients with intestinal failure requiring total parenteral nutrition use.


Outcome Measures
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Primary Outcome Measures :
  1. All cause mortality [ Time Frame: Up to 1427 days ]

Eligibility Criteria
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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients requiring total parenteral nutrition during in hospital admission.
Criteria

Inclusion Criteria:

  • all consecutive patients on TPN

Exclusion Criteria:

  • patients from the Pediatric and Haematological Departments
Contacts and Locations
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02189993


Locations
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Netherlands
Department of Gastroenterology and Hepatology, Small Bowel Unit, VU University Medical Center
Amsterdam, Netherlands
Sponsors and Collaborators
VU University Medical Center
Investigators
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Principal Investigator: Leendert Oterdoom, MD PhD VUMC
More Information
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Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

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Responsible Party: Leendert Oterdoom, Dr., VU University Medical Center
ClinicalTrials.gov Identifier: NCT02189993    
Other Study ID Numbers: TPN-01
First Posted: July 15, 2014    Key Record Dates
Last Update Posted: July 17, 2014
Last Verified: July 2014
Keywords provided by Leendert Oterdoom, VU University Medical Center:
Mortality
Long term follow-up
Parenteral Nutrition, Total
Additional relevant MeSH terms:
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Nutrition Disorders