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Post-pyloric Feeding and Feeding Intolerance in ARDS Patients Receiving Prone Position Ventilation

Post-pyloric Feeding and Feeding Intolerance in ARDS Patients Undergoing Prone Position Ventilation: a Single-center, Retrospective Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07421635
Enrollment
319
Registered
2026-02-19
Start date
2016-07-30
Completion date
2024-12-30
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Clinical Outcomes

Brief summary

Evidence remains limited regarding the optimal enteral nutrition (EN) route for acute respiratory distress syndrome (ARDS) patients undergoing prone positioning. This study aimed to explore the association of post-pyloric feeding with feeding intolerance (FI), specifically in that population.

Detailed description

This single-center retrospective study included adult patients with ARDS who received prone position ventilation at Zhongda Hospital, Southeast University, between July 30, 2016, and April 30, 2024. The primary outcome was the incidence of FI, defined as the failure to achieve an enteral energy intake of 17.5 kcal/kg/day within 72 hours of initiating EN. The statistical approaches utilized included multivariate regression, inverse probability weighting model, and marginal structural cox model to ensure the robustness of our findings. Subgroup analyses were also performed.

Interventions

None listed

Sponsors

Southeast University, China
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. age ≥ 18 years old 2. ARDS, defined by the Berlin standard 3. patients receiving prone position ventilation treatment

Exclusion criteria

1. No enteral nutrition within 4 days after initiation of invasive mechanical ventilation 2. Duration of invasive mechanical ventilation \<72 hours after initiation of enteral nutrition 3. Prone positioning initiated \>3 days after EN 4. Duration of each prone session \<12 hours 5. Severe acute pancreatitis 6. Contraindications to early enteral nutrition

Design outcomes

Primary

MeasureTime frameDescription
Incidence of FIat day 3Incidence of feeding intolerance during enteral nutrition within 72 hours of initiating EN

Secondary

MeasureTime frameDescription
Incidence of enteral nutrition-related complicationsup to 3 daysIncidence of feeding-related complications during enteral nutrition
ICU mortalityup to 24 monthsthe survival rate(survival/total) during ICU stay
28-day mortalityat day 28mortality in Day 28
VFDs at day 2828 daysdefined as the number of days between successful weaning from MV and day 28 after study enrollment
Length of ICU stayup to 24 monthsthe number of days from ICU admission to ICU discharge or death

Contacts

STUDY_DIRECTORling liu, phD

Department of Critical Care Medicine, Zhongda Hospital, School of Medicine, Southeast University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 31, 2026