Gastrointestinal Hormones and Metabolomic Profiling Following Mixed-Meal Tolerance Tests in Patients at Risk of Refeeding Syndrome

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorHospital Garcia de Orta

About this trial

Introduction: Refeeding syndrome (RS) is a life-threatening metabolic complication of nutritional support. Prolonged fasting, frequently observed in malnourished patients referred for percutaneous endoscopic gastrostomy (PEG), induces histological and ultrastructural changes in the intestinal mucosa, potentially influencing RS development. Mixed-Meal Tolerance Tests (MMTT) combined with metabolomics allow dynamic assessment of serum glucose, gastrointestinal hormones and cellular metabolites, which may help to elucidate RS pathogenesis and assess patient risk. Objective: The present study aims to perform MMTT in PEG-fed patients to evaluate enteroendocrine hormone responses and metabolomic profiles following a prolonged fasting period and subsequent enteral refeeding. Methods: This prospective, single-center study includes adults referred for PEG after at least one month of oral intake below 50% of energy needs. The MMTT will be performed at PEG placement and after 3-6 months of enteral nutrition. Serial blood samples will be collected from baseline up to 120 minutes post-meal to measure serum glucose, insulin, C-peptide, electrolytes and gastrointestinal hormones (GLP-1/GIP/Ghrelin/Peptide YY), and for metabolomic profiling by spectroscopy. Clinical and nutritional data will be prospectively recorded. Statistical and multivariate analyses will assess metabolic and hormonal changes over time and their potential association with patient refeeding syndrome risk and clinical outcome. The study was approved by the institutional ethics committee, and patient informed consent will be obtained. Conclusion: This study integrates MMTT and metabolomic profiling to characterize hormonal and metabolic responses during fasting and refeeding in high-risk PEG patients. Findings are expected to reveal underlying mechanisms of RS, identify potential predictive biomarkers, and improve individualized risk stratification and nutritional management.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age above 18 years.

Oral ingestion below 50% of energy daily needs for ≥ 1 month.

Absence of artificial nutrition before PEG placement.

Disqualifiers

Age below 18 years.

Quantified food ingestion above 50% of energy daily needs during the last month.

Oncologic disease.

Diabetes mellitus.

Trial population

Ambulatory patients referred to PEG for long-term enteral nutrition.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

15 Participants
are grouped into 1 trial group
Group A: Ambulatory patients referred to percutaneous endoscopic gastrostomy for long-term enteral nutrition.

Trial outcomes

Primary outcomes

1

To define the kinetics of serum glucose, electrolytes and gastrointestinal hormones during fasting and refeeding.

Time frame
From enrollment to the end of the study at 3-6 months.
2

To perform MMTT and metabolomic analysis to patients referred for endoscopic gastrostomy after a significant period of low ingestion.

Time frame
At the time of the inclusion
3

To repeat the same evaluation after 3-6 months of long-term enteral nutrition with adequate energy supply.

Time frame
At 3-6 months after inclusion
4

To analyze the evolution of serum metabolites during fasting and refeeding aiming to identify potential predictive biomarkers of RS development in high-risk patients.

Time frame
From enrollment to the end of the study at 3-6 months.

Secondary outcomes

Other outcomes

Sponsors and contacts

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Hospital Garcia de Orta

Lead sponsor

Instituto de Ciências Biomédicas Abel Salazar

Collaborator

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