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Compassionate Use of Omegaven

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Geisinger Health

Status

Conditions

Cholestasis

Treatments

Dietary Supplement: Omegaven

Study type

Expanded Access

Funder types

Other

Identifiers

NCT02778698
OMEGAVEN

Details and patient eligibility

About

This expanded access protocol is for infants or children with conditions preventing them from taking in enough nutrients from food and must receive nutrition intravenously. Standard intravenous nutrition contains fat emulsion made from soybean. If this fat emulsion is given over a long period of time, it can cause problems within the liver and if persistent and not addressed can even lead to severe and/or permanent injury to the liver.

It is believed that a type of fish oil blend, called Omegaven®, may be used in place of the soybean fat blend. The Omegaven® fish oil blend may greatly reduce the risk of liver injury.

Omegaven® is not approved by the Food and Drug Administration (FDA). It is only offered under an "expanded access" protocol as an alternative to the soybean fat blend.

Sex

All

Ages

15 days to 5 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Male or female
  2. Older than 14 days and less than 5 years of age
  3. Direct bilirubin value is greater than 2 mg/dL
  4. Be expected to require intravenous nutrition for at least an additional 28 days
  5. Parent/legal guardian has agreed to provide consent/parental permission

Exclusion criteria

  1. Patients who have a congenitally lethal condition (e.g. Trisomy 13).
  2. Patients who have clinically severe bleeding not able to be managed with routine measures.
  3. Patients who have evidence of a viral hepatitis or primary liver disease as the primary etiology of their cholestasis.
  4. Patients who have other health problems such that survival is extremely unlikely even if the infant's cholestasis improves.

5 The parent/legal guardian is unwilling to provide consent/parental permission.

Trial contacts and locations

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Data sourced from clinicaltrials.gov

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