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OpenTrials
Completed

NCT Number: NCT00647036

Microbial Invasion During Parenteral Nutrition in Surgical Infants Receiving Glutamine

We hypothesise that the addition of glutamine supplementation to both parenteral nutrition and enteral feeds in surgical newborn infants leads to a reduction in bacterial invasion.

Completed

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Key information

Conditions

Surgical Infants Requiring Total Parenteral Nutrition Hyperphagia Pathological Conditions, Signs and Symptoms Signs and Symptoms Signs and Symptoms, Digestive

Age range

Up to 3 month

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Institute of Child Health, 30 Guilford Street

London, WC1N 1EH, United Kingdom

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Infants who have undergone surgical procedures for congenital anomalies or
  • Intestinal inflammation who require total parenteral nutrition.

Exclusion criteria

-

Treatment and study plan

Isonitrogenous Vaminolact

Dietary Supplement

Isonitrogenous Vaminolact

Dipeptiven (L-glutamine- Lalanine)

Drug

0.6g/kg/day

Primary outcomes

  1. Evidence of microbial invasion

    Time frame: 5 days

Interested in participating?

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Sponsors and collaborators

Lead sponsor

Institute of Child Health

Other

Registry information

Official study title

Microbial Invasion During Parenteral Nutrition in Surgical Infants Receiving Glutamine.

Important dates

Study start
2009
Primary completion
2011
Study completion
2012
First posted
Mar 31, 2008
Registry last updated
Jan 25, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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