Fortimel Taste Optimization in Oncology Patients for Nutritional Support
Fortimel
Neoplasms
Supportive Care Study
Summary
Study start date: December 1, 2024
Actual date on which the first participant was enrolled.This study aims to explore the use and effectiveness of a nutritional drink called Fortimel, specifically designed for cancer patients. These patients often require special nutritional support to maintain their health during treatment. The study focuses on how well patients tolerate different flavors of this drink and whether it improves their overall nutrition and quality of life. By observing how patients react to this drink in a real-world setting, the study seeks to enhance the nutritional care for oncology patients, potentially leading to better compliance with dietary recommendations and improved health outcomes. Participants in this study will receive a ready-to-drink formula, provided in four different flavors over a 28-day period, with one or two bottles consumed daily. Throughout the study, the nutritional status and quality of life of the patients are assessed at various points before and after they start drinking the formula. To help participants stick to the regimen, a support platform offers guidance on nutrition and diet. The study involves a follow-up period lasting up to 60 days after the intervention, ensuring that the effects of the nutritional support are carefully monitored and documented.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.2000 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 80 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Dongcheng district,Peking union medical college hospital
Beijing, ChinaOpen Dongcheng district,Peking union medical college hospital in Google Maps