Methionine Metabolism in Enterally Fed Pediatric Sepsis

Sepsis Clinical Trial

Official title:

Methionine Metabolism in Enterally Fed Critically Ill Children

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01889264
• Other study ID #: STU-042011-088
• Status: Completed
• Phase: N/A
• First received: May 24, 2013
• Last updated: March 20, 2017
• Start date: December 2011
• Est. completion date: October 2016

Study information

• Verified date: March 2017
• Source: The Cleveland Clinic
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Critically ill children have abnormal utilization of nutrients such as glucose, lipids and protein. Protein synthesis is increased mainly in the form of immune and signaling proteins, while muscle and structural protein synthesis is decreased. The metabolism of sulfur amino acids through the splanchnic area and specifically methionine and cysteine have not been investigated in critically ill septic children, despite that sulfur amino acids have important roles in thiol, antioxidant and epigenetic reactions. Methionine metabolism in sick children will be influenced by its rate of utilization through different pathways. Our study aims to investigate the metabolism of methionine and cysteine when both amino acids are given by the enteral route in critically ill septic children. The investigators are focused on the rates of transmethylation, remethylation and transsulfuration in critically ill septic children, and if the current standard nutrition maintains methionine nutritional balance and functional requirements in critically ill children fed by the enteral route.

Description:

This is a prospective, translational study on the splanchnic metabolism of methionine to determine the rates of the different pathways and synthesis rates of glutathione when critically ill children are fed by the enteral route, and the difference among various age groups. The study size will include 45 critically ill septic, pediatric patients (15 infants at 1 month-3 years of age, 15 children at 4-12 years of age and 15 adolescent at 13-19 years of age), males and females admitted to the pediatric intensive care unit (PICU) at Children's Medical Center, Dallas. The minimal subject's weight will be 4 kg. The number of subjects includes an expected drop out rate of about 20%, in order to obtain 15 patients with complete data in each group. Patients will receive nutritional support as per standard care. This study will yield important knowledge and may lead in the future to changes in the current practice on the management of critically ill pediatric patients in the PICU.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 45
• Est. completion date: October 2016
• Est. primary completion date: October 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 1 Month to 19 Years

Eligibility

Inclusion Criteria:

1. Children age 1 month-19 years

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:

1. Patients with metabolic diseases (i.e. Insulin dependent diabetes mellitus, urea cycle disorders, cystinuria, etc.)

2. Pregnancy

3. Primary liver failure

4. Primary renal failure

5. Patients unable to tolerate enteral feedings

6. Weight less than 4.0 kg

Related Conditions & MeSH terms

• Critical Illness
• Sepsis

Intervention

Other:
• Observational
Observational, Translational non-treatment study

Locations

Country	Name	City	State
United States	Cleveland Clinic	Cleveland	Ohio

Sponsors (1)

Lead Sponsor	Collaborator
The Cleveland Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Methionine Metabolism	Rates of transmethylation, remethylation and transsulfuration and erythrocyte GSH synthesis when nutrients are given by the enteral route in pediatric critically ill patients.	Clinical Signs, AEs, SAEs, CO2, Tracer Infusion, Blood: (Baseline - 8 hours)