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DeliKet (Substudy of KetoNiFast Study ID 22-1398_1)

Impact of Cyclic, Daytime Enteral Nutrition and Ketogenic Nighttime Fasting on the Incidence of Postoperative Delirium in Critically Ill Patients

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06535022
Acronym
DeliKet
Enrollment
90
Registered
2024-08-02
Start date
2024-09-01
Completion date
2026-03-01
Last updated
2024-08-06

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

Conditions

Delirium, Ketogenic Dieting, Nutrition, Healthy

Keywords

ketogenic diet, cyclic nutrition, postoperative delirium

Brief summary

Postoperative delirium is a common problem of the critically ill patient and associated with an increased mortality. Intermittent fasting and ketogenesis have been shown to be beneficial for maintaining a circadian rhythm and initiating anti-inflammatory repair mechanisms which could potentially be neuroprotective. However, so far there is little data if cyclic enteral feeding with ketogenic nighttime fasting might be beneficial for reducing the rate of postoperative delirium. The study hypothesis is that equicaloric cyclic enteral feeding (12 hrs) during daytime with ketogenic fasting and exogenous ketone supplementation at nighttime compared to continuous standard enteral nutrition (24 hours) decreases the incidence of postoperative delirium in critically ill patients.

Detailed description

Postoperative delirium remains a common postoperative problem in critically ill patients with a prevalence of up to 20% and even up to 50% in the elderly population. But postoperative delirium has a negative impact on mortality as several studies were able to show in the past. Therefore, aiming for a reduction of postoperative delirium has an important impact on patients' outcome. One helpful tool for avoiding postoperative delirium is maintaining a circadian pattern. Enteral feeding may play an important role here. Healthy humans have a circadian feeding pattern with nighttime fasting. There is increasing evidence that a circadian rhythm of feeding (cyclic feeding) could be beneficial for critical ill patients. Cyclic feeding and fasting are assumed to have positive effects on the gut microbiome resulting in optimization of host responses to gastrointestinal pathogens. Another positive effect of cyclic feeding potentially results from activation of a fasting response, inducing repair pathways such as ketogenesis, mitochondrial biogenesis, anti-inflammatory pathways, antioxidant defenses and autophagy processes. The activation of these repair pathways could diminish cellular stress and promote cellular recovery in critical ill patients. This could have a positive effect on postoperative delirium. A randomized controlled trial by van Dyck et al. could show that fasting-mimicking intervals of 12 hours are sufficient to generate a metabolic fasting response without risking a caloric deficit. This fasting response can be enhanced by additional supplementation of exogenous ketones. The study objective is that equicaloric cyclic enteral feeding (for 12 hours) during daytime with ketogenic fasting (for 12 hours) at nighttime (aiming for a ß-hydroxybutyrate blood concentrations ≥ 0.5mM by exogenous ketone supplementation) compared to continuous (for 24 hours) standard enteral nutrition as per patients' nutritional requirements decreases the incidence of postoperative delirium of critically ill patients.

Interventions

DIETARY_SUPPLEMENTCyclic enteral daytime feeding with ketogenic nighttime fasting and exogenous ketone salt supplementation (ß-hydroxybutyrate)

Nighttime fasting and ß-hydroxybutyrate supplementation

Sponsors

University Hospital of Cologne
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Masking description

sealed, opaque envelopes

Intervention model description

Prospective, randomized, monocentric, interventional study

Eligibility

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

Inclusion criteria

* Age ≥ 18 years * Admission to an ICU * Start of enteral nutrition

Exclusion criteria

* Severe liver insufficiency / liver disease (Child Pugh \> B or 7-9 points) * Post total Pancreatectomy / Insulin-depending diabetes mellitus (IDDM) * Pregnancy / Lactation * Hemoglobin-concentration \< 80g/l * Severe metabolic disorder / severe autoimmune disease * Refractory respiratory or metabolic acidosis * Disorder of mitochondrial transportation of fatty acids * Disorder of the oxidation of fatty acids * Disorder of gluconeogenesis, der ketone body production or ketone body degradation * Intermittent porphyria * Severe arrhythmia / cardiomyopathy * Contraindications against enteral nutrition * Missing informed consent

Design outcomes

Primary

MeasureTime frameDescription
Confusion Assessment Method (CAM- ICU)Day 1-14 after randomization or until ICU dischargeCAM ICU score (lowest score 0, highest score 7) • Cognitive function (MoCA- and MMST- Score) day 1, 7, 14 / ICU discharge
• Montreal Cognitive Assessment (MoCA- Score)Day 1-14 after randomization or until ICU- discharge• Cognitive function (MoCA- Score) (lowest Score 0, highest Score 30)
MMSE (Minimental State Examination)Day 1-14 after randomization or until ICU dischargeMMSE Score (lowest Score 0, highest Score 30)

Secondary

MeasureTime frameDescription
Duration of ventilationFrom day of randomization until ICU discharge up to 1 monthLength of invasive and noninvasive ventilation
Length of ICU- and Hospital stayFrom day of randomization until hospital discharge up to 6 monthsLength of ICU- and Hospital stay
30-day mortalityFrom day of randomization up until 30 daysMortality at day 30 after ICU admission

Contacts

Primary ContactSandra E Stoll, MD, assProf.
sandraemilystoll@googlemail.com+49221478
Backup ContactFabian Dusse, PD, MD
fabian.dusse@uk-koeln.de+49221478

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026