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NCT06741761 · ClinicalTrials.gov registry record · NA
12-hour Time Limited Feeding in Critical Care
A NA study of Critical Illness, sponsored by University of Kansas Medical Center.
- Recruiting
- Registry status
- NA
- Development phase
- 20
- Enrollment target
- 1
- Study location
NCT06741761 is a NA study of Critical Illness that is actively recruiting participants, run by University of Kansas Medical Center. The registered enrollment target is 20 participants, below the 3,138-participant average among 91 other Critical Illness trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06741761, a NA study of Critical Illness, is actively recruiting participants, sponsored by University of Kansas Medical Center.
- RECRUITING
- Registry status
- NA
- Development phase
- 20 participants
- Enrollment target
- 1
- Study location
Study Summary
This study is being done to assess the feasibility and safety of a time-restricted 12-hour enteral feeding protocol (experimental group) in comparison to a standard-of-care, 24-hour enteral feeding protocol (control group) in critically ill patients. Investigators hope to gain knowledge about how these feeding schedules affect feeding tolerance, blood sugar control, and other factors affecting critically ill adult patients. * Investigators expect that the 12-hour feeding protocol will be tolerated similarly to the 24-hour feeding protocol and will not result in a greater number of adverse events related to feeding. * Investigators expect that the proportion of participants in both groups receiving at least 75% of their estimated nutrition needs will be similar.
Conditions Studied
Interventions
- OTHER 12-hour time-restricted feeding (TRF12)
- OTHER Continuous 24 hour feeding (CONT24).
Study Locations (1)
Kansas
- University Of Kansas Health System - Kansas City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2025-03-25 |
| Est. Completion | 2026-06 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06741761
The ClinicalTrials.gov registry entry for NCT06741761 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 3,138-participant average among 91 other Critical Illness trials with a reported enrollment target (99% lower). The listed sponsor is University of Kansas Medical Center, which has 408 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Critical Illness appearing as the primary indexed condition, and to 2 interventions - of which 12-hour time-restricted feeding (TRF12) is the first listed.
NCT06741761 reports 1 study location spanning 1 distinct geographic area - top geographies include Kansas.
Frequently Asked Questions
What is clinical trial NCT06741761 about?
NCT06741761 is a clinical study titled "12-hour Time Limited Feeding in Critical Care". This study is being done to assess the feasibility and safety of a time-restricted 12-hour enteral feeding protocol (experimental group) in comparison to a standard-of-care, 24-hour enteral feeding protocol (control group) in critically ill patients. Investigators hope to gain knowledge about how th...
What is the current status of trial NCT06741761?
This trial is currently recruiting. It is a NA study. The enrollment target is 20 participants. The study started on 2025-03-25. Estimated completion is 2026-06.
What conditions does trial NCT06741761 study?
This clinical trial studies the following conditions: Critical Illness.
What interventions are being tested in trial NCT06741761?
The interventions under investigation include: 12-hour time-restricted feeding (TRF12) (OTHER), Continuous 24 hour feeding (CONT24). (OTHER).
Who is sponsoring clinical trial NCT06741761?
This trial is sponsored by University of Kansas Medical Center, which has 408 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06741761 being conducted?
This trial has 1 study location across Kansas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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