Effect of Intermittent Enteral Feeding in Severe Stroke

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorXijing Hospital

About this trial

This is a single-center, randomized, exploratory clinical trial investigating whether intermittent enteral feeding improves outcomes compared to continuous feeding in patients with severe stroke. The study will enroll 60 patients to evaluate the impact on 90-day all-cause mortality, neurological function, nutritional status, and safety. It will also explore underlying mechanisms through analysis of metabolic profiles, circadian gene expression, and gut microbiota.

Eligibility criteria

Qualifiers

Age ≥18 years old

It was definitely diagnosed as acute stroke by clinical imaging.

Enteral nutrition program can be started within 72 hours of onset.

Baseline GCS≤12 or NIHSS≥11

Disqualifiers

Before joining the group, he had received total parenteral nutrition treatment.

There are contraindications to enteral nutrition.

Unstable vital signs

Dementia or severe disability before onset (mRS≥3)

Trial design

Treatments tested in this trial

  • Intermittent Enteral Feeding
  • Continuous Enteral Feeding

Treatment groups

60 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators