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Can better nutrition guidelines save lives in the ICU?

NCT ID NCT07337798

Knowledge-focused Sponsor: Xuanwu Hospital, Beijing Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at whether a new, evidence-based nutrition guideline can improve care for patients in surgical intensive care units (ICUs). About 200 healthcare workers from Chinese hospitals will use the guideline and be checked for how well they follow it. The goal is to see if patients get the right amount of energy and protein during their ICU stay. This is a quality improvement study, not a treatment trial.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 200 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Dec 2025

An estimate. Start dates often move.

Expected to finish

Dec 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: For ICU healthcare professionals: Employed at one of the participating study sites (tertiary general hospitals) Holds a valid Registered Nurse license issued in the People's Republic of China Currently working in frontline clinical nursing care in a surgical intensive care unit (ICU) during the study period At least 1 year of clinical working experience Able to understand the study objectives and procedures Willing to participate and able to provide written informed consent For surgical critically ill patients (outcome assessment population): Aged 18 years or older Admitted to a surgical ICU due to surgical-related conditions, including trauma, infection, malignancy, or postoperative complications Expected length of stay in the surgical ICU of at least 48 hours No restriction on sex Patient or legally authorized representative able to provide written informed consent Exclusion Criteria: For ICU healthcare professionals: Currently pregnant, breastfeeding, or planning pregnancy during the study period Temporarily assigned, rotating, externally dispatched, on long-term training, or on leave during the study period, making continuous participation impossible Participation in other interventional studies that may interfere with the implementation of this study Determined by the research team to have cognitive, communication, or other conditions that would make participation inappropriate For surgical critically ill patients: Diagnosed with brain death or awaiting organ donation Pregnant or breastfeeding women Concurrent participation in other nutrition-related clinical trials

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Enteral nutrition Enteral nutrition intolerance Icu patients Nutrition intervention Surgical

How to take part

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  1. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  2. A doctor treating you

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