Transcutaneous Auricular Stimulation Targeting Enteral Feeding Intolerance (TASTE-FI)
Efficacy of Transcutaneous Auricular Vagus Nerve Stimulation for Enteral Feeding Intolerance in Critically Ill Patients in the Intensive Care Unit: A Single-Center, Single-Blind, Randomized Controlled Trial
This study will test whether electrical stimulation applied to the outer ear can improve tolerance of tube feeding in critically ill adults in the intensive care unit (ICU). Some ICU patients develop digestive problems, such as vomiting, diarrhea, or a buildup of feeding liquid in the stomach. These problems can prevent them from receiving enough nutrition through a feeding tube. This is called enteral feeding intolerance.
The treatment being studied is called transcutaneous auricular vagus nerve stimulation (taVNS). It delivers small electrical pulses through electrodes placed on the skin of the outer ear, usually the left ear. It does not require surgery. The treatment targets a branch of the vagus nerve, which helps regulate digestion. Researchers want to find out whether adding this treatment to usual ICU care improves feeding tolerance and whether it causes side effects.
The study will enroll 60 adults aged 18 years or older with enteral feeding intolerance at one hospital. Participants will be assigned by chance to one of two groups, with an equal chance of joining either group:
- Usual ICU care alone.
- Usual ICU care plus ear stimulation for 60 minutes once daily for five days.
Stimulation will stop earlier if a participant leaves the ICU or the study team determines that it should be stopped for safety reasons.
The main measure will be the proportion of participants whose feeding intolerance improves between 24 and 120 hours after enrollment. Improvement means receiving the study's target amount of calories through tube feeding for at least 48 consecutive hours without stopping feeding because of intolerance.
Researchers will also collect blood samples and rectal swabs to study intestinal function, gut bacteria, and substances produced by the body and gut bacteria. They will record the use of pain medicines and sedatives, changes in illness severity, and possible side effects, including skin irritation, a slow heartbeat, or low blood pressure.
Study assessments and sample collection in the ICU will continue for up to seven days after enrollment, ending earlier if the participant leaves the ICU.
Follow-up at 28 and 90 days will assess survival and, at 90 days, new infections and hospital readmissions.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Estimé)
Phase
- N'est pas applicable
Contacts et emplacements
Lieux d'étude
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Wuhan, Chine
- Department of Critical Care Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
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Contact:
- Jiancheng Zhang
- E-mail: zhjcheng1@126.com
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- Age ≥18 years;
- Admission to the intensive care unit (ICU), with an expected ICU stay of at least 5 days;
- Enteral nutrition has been initiated or is planned;
- At least one of the following manifestations of gastrointestinal dysfunction: (1) Intra-abdominal hypertension: intra-abdominal pressure ≥12 mmHg on at least two measurements within 6 hours, or a mean pressure ≥12 mmHg based on at least four measurements within 24 hours; (2) Gastric retention: gastric residual volume >200 mL on a single aspiration; (3) Diarrhea: more than three loose or watery stools per day, with a total volume >250 mL/day; (4) Lower gastrointestinal paralysis: no bowel movement for at least 3 days, with bowel sounds present or absent, after exclusion of mechanical bowel obstruction; (5) Bowel dilatation on abdominal radiography, computed tomography, or bedside ultrasound: colonic diameter >6 cm, cecal diameter >9 cm, or small bowel diameter >3 cm;
- Enteral feeding intolerance confirmed during a 72-hour trial of enteral nutrition guided by the study's feeding intolerance assessment: failure to achieve an enteral energy intake of 20 kcal/kg/day within 72 hours, or discontinuation of enteral nutrition for a clinical reason, such as vomiting, diarrhea, gastrointestinal bleeding, or an intestinal fistula. Temporary interruptions for clinical procedures do not qualify;
- Written informed consent provided by the participant or a legally authorized representative.
Exclusion Criteria:
- An absolute contraindication to enteral nutrition, including but not limited to intestinal ischemia, gastrointestinal perforation, complete bowel obstruction, or active major gastrointestinal bleeding;
- Severe cardiac arrhythmia or high-grade atrioventricular block;
- An implanted cardiac pacemaker, implantable cardioverter-defibrillator, or other implanted electronic device;
- Local infection, ulceration, skin injury, or another condition affecting the outer ear that makes transcutaneous auricular vagus nerve stimulation unsuitable;
- Pregnancy or breastfeeding;
- Expected death within 24 hours or receipt of end-of-life care.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Seul
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Aucune intervention: Groupe de contrôle
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Expérimental: taVNS intervention group
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Transcutaneous auricular vagus nerve stimulation will be delivered through surface electrodes over the cymba conchae and cavum conchae, preferably of the left ear, alongside standard ICU care. Stimulation parameters are 25 Hz, a pulse width of 200-500 microseconds, and an individually adjusted current, typically 0.5-2.0 mA. Sessions will last 60 minutes once daily for five consecutive days. Heart rate, blood pressure, and local skin reactions will be monitored. Stimulation will stop for intolerance or safety concerns and end early upon ICU discharge. |
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Enteral Feeding Intolerance Response Rate
Délai: 24-120 hours after enrollment
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Percentage of participants who achieve an enteral energy intake of at least 20 kcal/kg/day for at least 48 consecutive hours within the assessment window, without interruption of enteral feeding due to intolerance. |
24-120 hours after enrollment
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Change in Serum Citrulline Concentration
Délai: Within 24 hours before enrollment and 24-120 hours after enrollment.
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Change from baseline in serum citrulline concentration, used as a marker of intestinal function. |
Within 24 hours before enrollment and 24-120 hours after enrollment.
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Change in Gut Microbial Diversity Measured by the Shannon Index
Délai: Within 24 hours before enrollment, 120 hours, and 168 hours after enrollment.
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Change from baseline in the Shannon diversity index of gut microbiota assessed using rectal swab samples. Higher values indicate greater microbial diversity. |
Within 24 hours before enrollment, 120 hours, and 168 hours after enrollment.
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Change in Gut Microbial Richness Measured by the Chao1 Index
Délai: Within 24 hours before enrollment, 120 hours, and 168 hours after enrollment.
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Change from baseline in the Chao1 richness index of gut microbiota assessed using rectal swab samples. Higher values indicate greater estimated microbial richness. |
Within 24 hours before enrollment, 120 hours, and 168 hours after enrollment.
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Changes in Gut Microbial Community Composition
Délai: Within 24 hours before enrollment, 120 hours, and 168 hours after enrollment.
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Differences in gut microbial community composition over time and between groups, assessed using Bray-Curtis dissimilarity in rectal swab samples. Higher values indicate greater differences between microbial communities. |
Within 24 hours before enrollment, 120 hours, and 168 hours after enrollment.
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Changes in Relative Abundance of Gut Microbial Taxa
Délai: Within 24 hours before enrollment, 120 hours, and 168 hours after enrollment.
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Changes from baseline in the relative abundance of gut microbial taxa at the phylum and genus levels, measured in rectal swab samples. Relative abundance is expressed as a percentage. |
Within 24 hours before enrollment, 120 hours, and 168 hours after enrollment.
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Changes in relative abundance of metabolites in rectal swab samples measured by liquid chromatography-tandem mass spectrometry
Délai: Within 24 hours before enrollment, 120 hours, and 168 hours after enrollment.
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Changes from baseline in metabolite abundances measured by metabolomic analysis of rectal swab samples. |
Within 24 hours before enrollment, 120 hours, and 168 hours after enrollment.
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Changes in relative abundance of metabolites in plasma samples measured by liquid chromatography-tandem mass spectrometry
Délai: Within 24 hours before enrollment, 120 hours, and 168 hours after enrollment.
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Changes from baseline in metabolite abundances measured by metabolomic analysis of plasma samples. |
Within 24 hours before enrollment, 120 hours, and 168 hours after enrollment.
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Opioid Analgesic Use
Délai: From enrollment through 120 hours after enrollment, or ICU discharge if earlier.
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Cumulative and mean daily opioid doses, expressed as intravenous morphine equivalents in mg and mg/day, respectively. |
From enrollment through 120 hours after enrollment, or ICU discharge if earlier.
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Propofol Use
Délai: From enrollment through 120 hours after enrollment, or ICU discharge if earlier.
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Cumulative and mean daily propofol doses, expressed in mg and mg/day, respectively. |
From enrollment through 120 hours after enrollment, or ICU discharge if earlier.
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Benzodiazepine Use
Délai: From enrollment through 120 hours after enrollment, or ICU discharge if earlier.
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Cumulative and mean daily benzodiazepine doses, expressed as intravenous midazolam equivalents in mg and mg/day, respectively. |
From enrollment through 120 hours after enrollment, or ICU discharge if earlier.
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Change in Sequential Organ Failure Assessment Score
Délai: Within 24 hours before enrollment and 24-120 hours after enrollment.
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Change from baseline in the Sequential Organ Failure Assessment (SOFA) score. Scores range from 0 to 24, with higher scores indicating more severe organ dysfunction. A negative change indicates improvement. |
Within 24 hours before enrollment and 24-120 hours after enrollment.
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Change in Acute Physiology and Chronic Health Evaluation II Score
Délai: Within 24 hours before enrollment and 24-120 hours after enrollment.
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Change from baseline in the Acute Physiology and Chronic Health Evaluation II (APACHE II) score. Scores range from 0 to 71, with higher scores indicating greater illness severity. A negative change indicates improvement. |
Within 24 hours before enrollment and 24-120 hours after enrollment.
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Vasoactive Medication Use
Délai: Within 24 hours before enrollment and 24-120 hours after enrollment.
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Percentage of participants receiving any vasoactive medication during each assessment period. |
Within 24 hours before enrollment and 24-120 hours after enrollment.
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Change in C-Reactive Protein Concentration
Délai: Within 24 hours before enrollment and 24-120 hours after enrollment.
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Change from baseline in blood C-reactive protein concentration, a marker of inflammation. |
Within 24 hours before enrollment and 24-120 hours after enrollment.
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Change in Procalcitonin Concentration
Délai: Within 24 hours before enrollment and 24-120 hours after enrollment.
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Change from baseline in blood procalcitonin concentration. |
Within 24 hours before enrollment and 24-120 hours after enrollment.
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Occurrence of ICU Delirium
Délai: up to 28 days after enrollment.
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Percentage of participants with at least one positive delirium assessment using the Confusion Assessment Method for the ICU (CAM-ICU) during the observation period. |
up to 28 days after enrollment.
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ICU Mortality
Délai: up to 28 days after enrollment.
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Percentage of participants who die from any cause during the ICU stay in which they are enrolled. |
up to 28 days after enrollment.
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In-Hospital Mortality
Délai: up to 90 days after enrollment.
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Percentage of participants who die from any cause during the hospitalization in which they are enrolled. |
up to 90 days after enrollment.
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28-Day All-Cause Mortality
Délai: From enrollment through Day 28.
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Percentage of participants who die from any cause within 28 days after enrollment. |
From enrollment through Day 28.
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90-Day All-Cause Mortality
Délai: From enrollment through Day 90.
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Percentage of participants who die from any cause within 90 days after enrollment. |
From enrollment through Day 90.
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All-Cause Hospital Readmission Within 90 Days After Discharge
Délai: From discharge from the index hospitalization through 90 days after discharge.
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Percentage of participants discharged alive from the index hospitalization who are readmitted to a hospital for any cause within 90 days after discharge. |
From discharge from the index hospitalization through 90 days after discharge.
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New Infections Within 90 Days
Délai: From randomization through Day 90.
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Percentage of participants who develop at least one new infection within 90 days after randomization, excluding infections present at ICU admission. |
From randomization through Day 90.
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Collaborateurs et enquêteurs
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Autres numéros d'identification d'étude
- zjc202605
Informations sur les médicaments et les dispositifs, documents d'étude
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