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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03646045
Other study ID # 741563-9
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date November 4, 2016
Est. completion date December 15, 2024

Study information

Verified date January 2024
Source Nemours Children's Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To determine the effect of transpyloric (TP) feeding on microaspiration and lung inflammation in ventilated preterm infants.


Description:

Specific Aim 1): To determine the effect of TP feeding on microaspiration and lung inflammation. Hypothesis: TP feeding will reduce the microaspiration and pulmonary inflammation in ventilated preterm infants. Evaluate markers of microaspiration (pepsin A) and lung inflammation [total cell counts, nuclear factor-kB (NF-kB) activation, tumor necrosis factor-α (TNF-α), IL-1β, IL-6, IL-8, angiopoietin 2 (Ang2), high-mobility group box-1 protein (HMGB1), macrophage migration inhibitory factor (MIF) and interferon-γ (IFN-γ)] in TA samples obtained from preterm ventilated infants with and without TP feeding. Specific Aim 2): To determine the effect of TP feeding on respiratory support. Hypothesis: TP feeding will decrease the respiratory severity score (RSS) [Fraction of inspired oxygen (FiO2) X mean airway pressure (MAP)] and number of infants requiring ventilator support. Evaluate respiratory support in preterm ventilated infants with and without TP feeding.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 46
Est. completion date December 15, 2024
Est. primary completion date May 30, 2018
Accepts healthy volunteers No
Gender All
Age group 0 Months to 12 Months
Eligibility Inclusion Criteria: - Preterm infants with birth weight <1500 grams - Requiring ventilatory support Exclusion Criteria: - Culture-proven sepsis - Ventilator associated pneumonia (VAP).

Study Design


Intervention

Other:
Transpyloric feeding
Preterm infant feeding using transpyloric feeding tube (nasoduodenal tube)

Locations

Country Name City State
United States Thomas Jefferson University Hospital Philadelphia Pennsylvania
United States AI duPont Hospital for Children Wilmington Delaware

Sponsors (1)

Lead Sponsor Collaborator
Nemours Children's Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Tracheal aspirate pepsin A levels in ventilated preterm infants receiving transpyloric feeding and gastric feeding. Difference in tracheal aspirate pepsin A levels in preterm ventilated infants receiving transpyloric feeding and gastric feeding. 3-7 days
Secondary Tracheal aspirate pepsin A levels in ventilated preterm infants before and after transpyloric feeding. Change in tracheal aspirate pepsin A levels in preterm ventilated infants before and after transpyloric feeding. 3-7 days
Secondary Tracheal aspirate cytokines levels (TNF-a, IL-1ß, IL-6, IL-8, Ang2, HMGB1, MIF and IFN-gamma) in ventilated preterm infants receiving transpyloric feeding and gastric feeding. Difference in tracheal aspirate cytokines levels (TNF-a, IL-1ß, IL-6, IL-8, Ang2, HMGB1, MIF and IFN-gamma) in preterm ventilated infants receiving transpyloric feeding and gastric feeding. 3-7 days.
Secondary Tracheal aspirate cytokines levels (TNF-a, IL-1ß, IL-6, IL-8, Ang2, HMGB1, MIF and IFN-gamma) in ventilated preterm infants before and after transpyloric feeding. Change in tracheal aspirate cytokines levels (TNF-a, IL-1ß, IL-6, IL-8, Ang2, HMGB1, MIF and IFN-gamma) in preterm ventilated infants before and after transpyloric feeding. 3-7 days
Secondary Respiratory support in ventilated preterm infants receiving transpyloric feeding and gastric feeding. Difference in respiratory severity score (FiO2 X mean airway pressure) in preterm ventilated infants receiving transpyloric feeding and gastric feeding. 7-14 days
Secondary Respiratory support in ventilated preterm infants before and transpyloric feeding. Change in respiratory severity score (FiO2 X mean airway pressure) in preterm ventilated infants before and after transpyloric feeding. 7-14 days
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