Impact of Specific Oligomeric Supplementation in Oncologic Patients Undergoing Radiotherapy With Malnutrition or at Risk.
NCT ID: NCT07035132
Last Updated: 2025-10-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ENROLLING_BY_INVITATION
132 participants
OBSERVATIONAL
2025-08-15
2025-12-31
Brief Summary
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Detailed Description
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To address malnutrition in these patients, international clinical guidelines recommend periodically reviewing their nutritional status and supplementing with oral nutrition formulas (ONS) when they are unable to meet their nutritional needs from their usual diet.
The ONSs have a nutrient composition designed to meet the specific needs of the patient, but there are pathologies, types of tumours and treatments, such as radiotherapy, chemotherapy, immunotherapy and others that can alter the digestion process, making it difficult for the gastrointestinal tract to utilise nutrients. Patients with these pathologies often cannot tolerate polymeric SNO formulations and require oligomeric peptide-based diet (PBD) formulations.
PBDs contain hydrolysed proteins in the form of peptides and medium-chain triglycerides (MCTs), which are more easily assimilated, helping patients to reduce weight loss and improve overall nutritional status. In addition, they contain hydrolysed serum lactoprotein with high biological quality that stimulates the formation of muscle tissue, minimising cachexia.
Radio/chemotherapy/immunotherapy treatment has negative effects on the nutritional and functional status of cancer patients, which also makes them more susceptible to the toxicities of cancer treatments and clinical complications. It has been shown that these patients tolerate PBD formulas well and even reduce their baseline intestinal symptoms, which facilitates compliance with nutritional treatment. However, adherence to these treatments remains a challenge as it is not always optimal, resulting in the non-achievement of the potential benefits.
The main objective of the study is to evaluate the effects of a hypercaloric SNO, with 100% hydrolysed serum lactoprotein and high MCT intake, in cancer patients undergoing radiotherapy, malnourished or at risk of malnutrition, in terms of improving the patient's nutritional status after 12 weeks of treatment.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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Oral supplementation with nutritional oligomeric formula
Patients will be supplemented with the specific oligomeric formula (1 or 2 bottles/day, as per investigator's decision) during, at least, the 12 weeks of the study follow-up.
Eligibility Criteria
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Inclusion Criteria
* Oncology patients (with head and neck, lung or rectal cancer) undergoing or about to start radiotherapy treatment. Patients with oesophageal cancer will also be included, as long as the patient is not undergoing PEG.
* Patients who are malnourished or at risk of malnutrition according to GLIM criteria.
* Patients requiring supplementation with an oligomeric formula with 100% hydrolysed serum lactoprotein and high MCT intake due to gastrointestinal disturbances (either maldigestion or maldigestion, malabsorption or dysmotility) intolerance to polymeric formulations or any other reason as considered by the physician.
* Patients who, at the discretion of the investigator, have the ability to answer the questionnaires and follow the procedures detailed in the protocol.
* Patients who give written informed consent to participate.
Exclusion Criteria
* Patients receiving nutritional support other than that of the study characteristics or who have received it during the last month. It will be accepted in patients who, being on a polymeric SNO, are advised to change to the oligomeric formula under study, due to gastrointestinal alterations, intolerances or any other reason considered by the doctor.
* Patients who have undergone surgery in the last three months.
* Patients who have received Enteral Nutrition in the last 3 months for SNG/SNJ/PEG.
* Pregnant or lactating women.
* Patients with advanced renal or hepatic disease (with creatinine clearance less than 45 ml/min or CP=C).
* Patients with advanced neoplastic disease with life expectancy \<3 months.
18 Years
ALL
No
Sponsors
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Nestlé Health Science Spain
INDUSTRY
Outcomes'10
NETWORK
Responsible Party
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Locations
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Hospital Universitario San Juan de Alicante
Alicante, , Spain
Hospital Universitario Fundación Jiménez Díaz
Madrid, , Spain
HU Clinica Asturias
Oviedo, , Spain
Hospital Universitario Son Espases
Palma de Mallorca, , Spain
Countries
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Other Identifiers
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NES-2023-154-PRO-PEP
Identifier Type: -
Identifier Source: org_study_id
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