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Cortagen

AEDP, Ala-Glu-Asp-Pro, Cortex Tetrapeptide

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Studies 14
Trials 43
Recruiting NA INTERVENTIONAL NCT06852014

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

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief 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.

Interventions

Name: Dietary Supplement: Experimental Treatment with nutritional suplement A + nutritional suplement B
Type: DIETARY_SUPPLEMENT
Description: Intervention group will receive a nutritional formula A and, after 1-week washout period, will receive a nutritional formula B
Name: Dietary Supplement: Dietary Supplement: Experimental Treatment with nutritional suplement B + nutritional suplement A
Type: DIETARY_SUPPLEMENT
Description: Intervention group will receive a nutritional formula B and, after 1-week washout period, will receive a nutritional formula A

Primary Outcomes

Measure: Adherence to nutritional treatment
TimeFrame: At weeks 6 and 13
Description: Categorized based on the average daily consumption compared to the prescribed volume (200 ml per bottle): * Full content (200 ml/bottle) * 2/3 content (150 ml/bottle) * 1/2 content (100 ml/bottle) * 1/4 content (50 ml/bottle) Patients will self-report their average daily consumption (ml/day).
Measure: Natural food intake
TimeFrame: At weeks 6 and 13
Description: Patients will report their food intake over the previous week, categorized into quartiles (%) relative to: * Pre-illness consumption * Perceived normal intake for patients without supplementation * ALL -100% * 3/4 - 75% * HALF - 50% * ¼ - 25% * NONE - 0%
Measure: Tolerance to nutritional treatment
TimeFrame: At weeks 6 and 13
Description: Evaluated based on the frequency of gastrointestinal symptoms (e.g., nausea, vomiting, reflux, abdominal pain, flatulence, satiety, constipation, and stomach heaviness) within two hours of supplement consumption. Symptoms classified as: * Never * Rarely * Sometimes * Frequently * Always Bivariate analysis will classify tolerance as: * Good (no symptoms) * Poor (presence of any gastrointestinal symptoms)
Measure: Change in aminoacids: Ala, Glu, Asp, Pro, Phe, Leu/Ile, Val, Tyr, Met, Cit, Arg, Gly, and Orn
TimeFrame: At baseline and in weeks 6, 7, and 13
Description: Aminoacids measured in µmol/L
Measure: Change in IL-6 and TNF-alpha RNA expression
TimeFrame: At baseline and in weeks 6, 7, and 13
Description: IL-6 and TNF-alpha measured from Peripheral blood mononuclear cell (PBMC)

Trial Information

NCT ID

NCT06852014

Status

Recruiting

Study Type

INTERVENTIONAL

Phases

NA

Sponsor

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

Last Updated

December 15, 2025

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