Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 4:58 PM
Ignite Modification Date:
2025-12-24 @ 4:58 PM
NCT ID:
NCT02538250
Eligibility Criteria:
Inclusion:
* Male and female patients
* ≥ 18 years of age
* Patients of the intended target group (e.g. MUST score ≥ 1) with an anticipated period of nutritional support ≥ 7 days
* Patient is able and willing to provide written informed consent
Exclusion:
* Hypersensitivity to milk, whey, soy, fish or any of the active substances or excipients
* Patients with available or potential impairment of sense of taste or smell due to disease (e.g. patients with cold, cancer patients) or medication (e.g. D-Penicillamine)
* Patients who express general dislike to two or more of the four flavours
* Severely impaired gastrointestinal function or complete failure
* Severe metabolic or circulatory disorders
* Acute disease
* Unstable vital functions
* Necessity of total parenteral nutrition or more than 50% Parenteral Nutrition in combined therapy
* Simultaneous participation in another interventional study
* Patients who are unwilling or mentally and/or physically unable to adhere to study procedures
* Pregnancy
* Emergencies
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02538250
Study Brief:
Protocol Section:
NCT02538250