Methionine Metabolism in Enterally Fed Pediatric Sepsis
NCT ID: NCT01889264
Last Updated: 2017-03-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
45 participants
OBSERVATIONAL
2011-12-31
2016-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Critically Ill Pediatric Patients
Critically ill septic pediatric patients, Age 1 month-3 years, Age 4-12 years and Age 13-19 years, males and females
Observational
Observational, Translational non-treatment study
Interventions
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Observational
Observational, Translational non-treatment study
Eligibility Criteria
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Inclusion Criteria
2. Diagnosis of severe sepsis diagnosed as clinical sepsis syndrome (requires two of the following criteria):
* Source of infection
* Fever or Hypothermia
* Leukocytosis or Leucopenia
* Poor organ perfusion (such as delayed capillary refill or decreased urine output or hypotension)
* Bacteremic sepsis demonstrated by positive blood culture
3. Weight greater or equal to 4.0 kg
4. Need for enteral nutrition by a nasogastric/nasoduodenal tube
5. Presence of central and/or arterial venous access as per clinical indication
Exclusion Criteria
2. Pregnancy
3. Primary liver failure
4. Primary renal failure
5. Patients unable to tolerate enteral feedings
6. Weight less than 4.0 kg
1 Month
19 Years
ALL
No
Sponsors
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The Cleveland Clinic
OTHER
Responsible Party
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Leticia Castillo
Department Chair Peds Critical Care
Principal Investigators
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Leticia Castillo, M.D.
Role: PRINCIPAL_INVESTIGATOR
The Cleveland Clinic
Locations
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Cleveland Clinic
Cleveland, Ohio, United States
Countries
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Other Identifiers
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STU-042011-088
Identifier Type: -
Identifier Source: org_study_id
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