RecruitingNot ApplicableNCT06852014

Effects of Peptamen 1.6 in Malnourished Patients (or at Risk) With Pancreatic Neoplasia Undergoing Cephalic Pancreaticoduodenectomy (CPD): A Mechanistic Study

Effects of Peptamen 1.6 in Malnourished Patients (or in Risk) With Pancreatic Neoplasia Undergoing Cephalic Pancreaticoduodenectomy (CPD): A Study Mechanistic.


Sponsor

Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina y Salud

Enrollment

20 participants

Start Date

May 29, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Malnutrition is a common challenge in patients with pancreatic cancer undergoing cephalic pancreaticoduodenectomy (CPD), impacting postoperative recovery and overall prognosis. Nutritional support plays a crucial role in optimising metabolic, inflammatory, and digestive outcomes. This randomised, double-blind, crossover clinical trial aims to evaluate the effects of Peptamen 1.6, a hydrolysed whey protein-based enteral formula, compared to Resource HP/HC, a high-protein and high-calorie polymeric formula, in malnourished or at-risk patients with pancreatic cancer undergoing PD. The study comprises both in vivo and in vitro analyses. The in vivo component will assess the impact of Peptamen 1.6 on digestive tolerance, amino acid absorption, nutritional status, metabolic profile, inflammatory markers, and gut microbiota composition. The in vitro component will utilise human intestinal organoid models to explore how enteral nutrition formulations influence intestinal permeability and metabolism, with a focus on microbiota interactions. Primary outcomes include improvements in metabolic status, assessed through serum biomarkers (albumin, immune markers, intestinal permeability, and myosin profile), inflammatory status via peripheral blood mononuclear cells (PBMCs), and microbiota shifts in faecal samples. Additionally, adherence to treatment, digestive tolerance, and changes in body composition will be monitored using bioelectrical impedance, dynamometry, and functional mobility tests. By elucidating the mechanisms through which different enteral nutrition strategies influence clinical, physiological, and molecular parameters, this study aims to enhance personalised nutritional interventions for patients with pancreatic cancer. The findings could contribute to optimising nutritional support strategies, ultimately improving patient outcomes following CPD.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests whether a specialized high-calorie nutritional formula (Peptamen 1.6) can help people recover better after surgery to remove a pancreatic tumor. It focuses on patients who are malnourished or at risk of malnutrition. **You may be eligible if:** - You have been diagnosed with cancer in or around the pancreas or duodenum - You recently had a Whipple procedure (a major surgery to remove part of the pancreas) - You had surgery within the last three months - You did not receive chemotherapy or radiation before surgery - You are not currently on other nutritional supplements or tube feeding **You may NOT be eligible if:** - You had your surgery more than three months ago - You have severe heart disease, kidney failure, or other serious health conditions - You have diarrhea caused by antibiotics or laxatives - You are pregnant or could become pregnant - You have diabetes with poorly controlled blood sugar (HbA1c above 8%) - You have a known allergy to components of the formula (e.g., galactosemia or fructosemia) Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIETARY_SUPPLEMENTDietary Supplement: Experimental Treatment with nutritional suplement A + nutritional suplement B

Intervention group will receive a nutritional formula A and, after 1-week washout period, will receive a nutritional formula B

DIETARY_SUPPLEMENTDietary Supplement: Dietary Supplement: Experimental Treatment with nutritional suplement B + nutritional suplement A

Intervention group will receive a nutritional formula B and, after 1-week washout period, will receive a nutritional formula A


Locations(1)

Hospital Regional Universitario de Málaga

Málaga, Málaga, Spain

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NCT06852014


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