Minayo Iron-rich Gummies for Female Anemia and Skin Health
Minayo Iron-rich Nutritional Gummies
+ Common Gummies
Anemia+2
+ Hematologic Diseases
+ Hemic and Lymphatic Diseases
Supportive Care Study
Summary
Study start date: March 17, 2025
Actual date on which the first participant was enrolled.This study is exploring the effects of Minayo Iron-rich Nutritional Gummies on women aged 18 to 45 who experience nutritional anemia, skin issues, and a condition known as Qi-blood deficiency syndrome. The research aims to determine if these gummies can improve anemia, which is checked by looking at specific blood levels like serum ferritin and hemoglobin. By focusing on this group, the study hopes to find better ways to manage these health challenges, potentially offering a simple nutritional solution to improve overall well-being and address specific symptoms associated with these conditions. Participants in this study are divided into two groups. One group receives the Minayo Iron-rich Nutritional Gummies, while the other receives regular gummies that have no active ingredients, known as a placebo. The study lasts for four weeks, during which participants visit the study center in Shanghai three times for evaluations. Researchers collect clinical data during these visits to analyze and compare the outcomes between the two groups. The main focus is to see if there is a noticeable improvement in anemia, skin conditions, and Qi-blood deficiency symptoms for those taking the Minayo gummies compared to the placebo group.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.36 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.Female
Biological sex of participants that are eligible to enroll.From 18 to 45 Years
Range of ages for which participants are eligible to join.Healthy volunteers 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
50% chance of being blinded to the placebo group
Treatment Groups
Group I
Active ComparatorGroup II
PlaceboStudy 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