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NCT07131098: EEFP

Early Enteral Feeding and Clinical Outcomes in ICU Patients

Completed NA Last updated 20 August 2025
What this trial tests

NA trial testing Early Enteral Feeding Protocol in Critical Illness in 80 participants. Completed in 30 April 2024.

Timeline
1 January 2024
Primary endpoint
30 April 2024
30 April 2024

Quick facts

Lead sponsorLoai Muawiah Zabin
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment80
Start date1 January 2024
Primary completion30 April 2024
Estimated completion30 April 2024
Sites1 location across Palestinian Territories

Drugs / interventions tested

Conditions studied

Sponsor

Loai Muawiah Zabin

Who can join

18 and older, any sex, with Critical Illness or Enteral Nutrition. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study evaluated the effectiveness of an early enteral feeding protocol in critically ill adult patients admitted to an Intensive Care Unit (ICU). The intervention involved initiating enteral nutrition within 24-48 hours of ICU admission. Clinical outcomes such as ICU length of stay, ventilator dependency, and selected laboratory values were compared between patients who received early enteral feeding and those who received standard nutritional care. The study was conducted at Jenin Governmental Hospital in Palestine between January and April 2024, with 80 adult participants.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Critical Illness

Currently open trials in the same condition.

Other Loai Muawiah Zabin trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07131098.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing