Effect of Krill Oil Supplementation on Red Blood Cell Physiology Against Changes in Markers of Iron Metabolism.
THYROX (Atlantic krill oil).
+ Placebo
Metabolic Diseases
+ Nutritional and Metabolic Diseases
+ Iron Metabolism Disorders
Basic Science Study
Summary
Study start date: March 23, 2024
Actual date on which the first participant was enrolled.This study investigates the effects of krill oil supplementation on red blood cell health and iron metabolism. Participants in this study include athletes or individuals who regularly engage in physical competition. The main aim is to understand how krill oil, which contains omega-3 fatty acids and other beneficial compounds, affects various blood markers and iron-related parameters in the body. This research is important as it could provide insights into how dietary supplements like krill oil can support optimal blood function and iron levels, potentially benefiting those with specific dietary needs or deficiencies. Participants are randomly assigned to two groups: one receives krill oil supplements, and the other receives a placebo, with neither the participants nor the researchers knowing who is in which group. The study lasts for six weeks, during which the krill oil group takes four capsules a day. Researchers measure various blood parameters, including complete blood counts and oxidative stress markers, using advanced laboratory techniques. These measurements help evaluate the effects of krill oil on red blood cell function and iron metabolism. The study is designed with safety in mind, although any potential risks associated with supplement intake are carefully monitored.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.30 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Basic Science 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 24 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.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
ExperimentalStudy Objectives
Primary 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
Poznań University of Physical Education
Poznan, PolandOpen Poznań University of Physical Education in Google Maps